Recombinant promoters and vectors for protein expression in liver and use thereof

ABSTRACT

Disclosed herein are recombinant viral vectors comprising a liver specific promotor in operable combination with a heterologous nucleic acid sequence encoding a protein, such as a clotting factor. Methods of treating a subject with a clotting disorder, such as hemophilia A or hemophilia B, are also provided.

CROSS REFERENCE TO RELATED APPLICATIONS

This is a continuation of U.S. application Ser. No. 16/058,808, filedAug. 8, 2018, which is a continuation of U.S. application Ser. No.15/128,912, filed Sep. 23, 2016, now U.S. Pat. No. 10,058,624, which isthe U.S. National Stage of International Application No.PCT/US2016/027931, filed Apr. 15, 2016, which was published in Englishunder PCT Article 21(2), which in turn claims the benefit of U.S.Provisional Application No. 62/202,133, filed Aug. 6, 2015, U.S.Provisional Application No. 62/212,634, filed Sep. 1, 2015, and U.S.Provisional Application No. 62/148,696, filed Apr. 16, 2015. Each of theprior patent applications is incorporated by reference herein in itsentirety.

ACKNOWLEDGMENT OF GOVERNMENT SUPPORT

This invention was made with government support under Grant Nos. RO1HL092179 U54 HL112309 awarded by the National Institutes of Health. Thegovernment has certain rights in the invention.

FIELD OF THE DISCLOSURE

This relates to recombinant promoters and vectors transgene expression,as well as recombinant nucleic acid molecules encoding novel clottingfactors.

BACKGROUND

Mutations in the clotting factor VIII (fVIII) gene result in a decreasedor defective clotting factor (fVIII) protein that gives rise tohemophilia A, which is characterized by uncontrolled bleeding.Hemophilia B is similarly associated with clotting factor IX (fix).Treatment of hemophilia A typically entails lifelong, multi-weeklyintravenous infusion of either human plasma-derived or recombinant fVIIIproduct. Due to the high cost, less than 30% of the global hemophilia Apopulation receives this form of treatment. Furthermore, about 25% ofpatients treated with fVIII replacement products develop neutralizingantibodies that render future treatment ineffective. Thus, there is aneed to identify improved therapies.

Gene therapies are typically based on genetically engineering virusesdesigned to deliver functional transgenes to the patient so that theirown cells can biosynthesize missing or defective proteins. Clinicaladvancements have been made using recombinant adeno-associated viral(rAAV) vectors for the expression of fIX in the liver; however, usingrAAV for fVIII expression for patients with hemophilia A has beenchallenging due to inefficient biosynthesis of human fVIII (hfVIII).Recombinant adeno-associated viral (rAAV) vectors produce capsids thathave a limited space for encapsulating nucleic acids. FVIII is a largeglycoprotein, and the rAAV sequences needed for encoding and expressingfVIII typically exceed capsid packing capacity.

SUMMARY

Disclosed herein are embodiments of a novel recombinant nucleic acidmolecule comprising a promoter that has been optimized to be of minimallength and to promote tissue-specific protein expression. In severalembodiments, the promoter can be a liver-specific promoter that promotessubstantially more protein expression in liver and liver cells than inother tissue types. In some embodiments, promoter can be included in aviral vector (such as an adeno-associated virus vector) in operablecombination with a heterologous nucleic acid sequence encoding a proteinof interest in order to promote expression of the protein of interest,for example in liver tissue and/or cells.

In some embodiments, the recombinant nucleic acid molecule can comprisea promoter comprising a first response element that comprises a set oftranscription factor (TF) binding sites including: a HNF1a TF bindingsite, a HNF1-1 TF binding site, a HNF4 TF binding site, a HNF3a TFbinding site, a HNF1-2 TF binding site, a HNF3-2 TF binding site, a HP1TF binding site, a TATA box; and a Transcription Start Site. In someembodiments, the HNF1a TF binding site comprises or consists ofnucleotides 1-12 of SEQ ID NO: 4; the HNF1-1 TF binding site comprisesor consists of nucleotides 16-23 of SEQ ID NO: 4; the HNF4 TF bindingsite comprises or consists of nucleotides 26-36 of SEQ ID NO: 4; theHNF3a TF binding site comprises or consists of nucleotides 39-45 of SEQID NO: 4; the HNF1-2 TF binding site comprises or consists ofnucleotides 48-62 of SEQ ID NO: 4; the HNF3-2 TF binding site comprisesor consists of nucleotides 65-71 of SEQ ID NO: 4; the HP1 TF bindingsite comprises or consists of nucleotides 75-87 of SEQ ID NO: 4; theTATA box comprises or consists of nucleotides 108-114 of SEQ ID NO: 4;and/or the Transcription Start Site (TSS) comprises or consists ofnucleotides 116-146 of SEQ ID NO: 4. In some embodiments, the firstresponse element can be of no more than 160 nucleotides in length (suchas no more than 150 nucleotides in length, such as 146 nucleotides inlength).

In some embodiments, the first response element comprises, from 5′ to3′, the HNF1a TF binding site, the HNF1-1 TF binding site, the HNF4 TFbinding site, the HNF3a TF binding site, the HNF1-2 TF binding site, theHNF3-2 TF binding site, the HP1 TF binding site, the TATA box, and theTranscription Start Site (TSS).

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 4 (HCB), or a sequence at least 90% identical thereto.

In some embodiments, the recombinant nucleic acid molecule can comprisea promoter comprising the first response element as discussed above, andcan further comprise a second response element. The second responseelement can comprise, for example, a HSh response element (for example,comprising or consisting of the nucleotide sequence set forth as SEQ IDNO: 111, or a sequence at least 90% identical thereto), a 5′HS responseelement (for example, comprising or consisting of the nucleotidesequence set forth as nucleotides 6-32 of SEQ ID NO: 111, or a sequenceat least 90% identical thereto), or a 3′ HS response element (forexample, comprising or consisting of the nucleotide sequence set forthas nucleotides 44-68 of SEQ ID NO: 111, or a sequence at least 90%identical thereto).

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas one of SEQ ID NO: 102 (HSh-HCB), SEQ ID NO: 104 (5′HSh-HCB), or SEQID NO: 103 (3′HSh-HCB), or a sequence at least 90% identical to one ofSEQ ID NO: 102 (HSh-HCB), SEQ ID NO: 104 (5′HSh-HCB), or SEQ ID NO: 103(3′HSh-HCB). In additional embodiments, the recombinant nucleic acidmolecule comprises a promoter comprising or consisting of the nucleicacid sequence set forth as one of SEQ ID NO: 5 (shortABP-HP1-God-TSS),SEQ ID NO: 7 (ABP-HP1-God-TSS), SEQ ID NO: 105 (HSh-SynO-TSS), SEQ IDNO: 106 (sHS-SynO-TSS), SEQ ID NO: 107 (Agro), SEQ ID NO: 108(HS-SynO-TSS), or SEQ ID NO: 112 (HNF1-ShortABPExact-SynO-TSS-Int), or asequence at least 90% identical to one of SEQ ID NO: 5(shortABP-HP1-God-TSS), SEQ ID NO: 7 (ABP-HP1-God-TSS), SEQ ID NO: 105(HSh-SynO-TSS), SEQ ID NO: 106 (sHS-SynO-TSS), SEQ ID NO: 107 (Agro),SEQ ID NO: 108 (HS-SynO-TSS), or SEQ ID NO: 112(HNF1-ShortABPExact-SynO-TSS-Int).

In some embodiments, promoter can be included in a vector, such as aviral vector (for example, an adeno-associated virus vector). In someembodiments, the promoter is included on the vector in operablecombination with a heterologous nucleic acid sequence encoding a proteinof interest in order to promote expression of the protein of interest,for example in liver tissue and/or cells. In some embodiments, theprotein of interest can be a clotting factor, such as fVIII or fiX orvariant thereof, such as a fVIII variant comprising fVIII A1, A2, A3,C1, and C2 domains, with the A2 and A3 domains joined by a peptidelinker, and deletion of the fVIII B domain. In some embodiments, theprotein of interest can be a fVIII variant and the heterologous nucleicmolecule can comprise or consist of the nucleic acid sequence set forthas SEQ ID NO: 2, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ IDNO: 126, or a nucleic acid sequence at least 90% identical to SEQ ID NO:2, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ ID NO: 126. Insome embodiments, the protein of interest can be a fIX and theheterologous nucleic molecule can comprise or consist of the nucleicacid sequence set forth as SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10,SEQ ID NO: 124, or SEQ ID NO: 127, or a nucleic acid sequence at least90% identical SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 124,or SEQ ID NO: 127.

In some embodiments, the vector can be a recombinant AAV vectorcomprising a genome comprising a nucleic acid molecule encoding any ofthe liver-specific promoters provided herein (such as the HCB promoter,SEQ ID NO: 4) operably linked to a heterologous nucleic moleculeencoding a fVIII variant, wherein the heterologous nucleic acid moleculecomprises or consists of the nucleic acid sequence set forth as SEQ IDNO: 2, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ ID NO: 126,or a nucleic acid sequence at least 90% identical to SEQ ID NO: 2, SEQID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ ID NO: 126. Is severalsuch embodiments, the recombinant AAV genome (from 5′ to 3′ ITR) is nomore than 5.1, 5.0, 4.9, 4.8, 4.7, 4.6, or 4.5 kb in length.

In some embodiments, the vector can be a recombinant AAV vectorcomprising a genome comprising a nucleic acid molecule encoding any ofthe liver-specific promoters provided herein (such as the HCB promoter,SEQ ID NO: 4) operably linked to a heterologous nucleic moleculeencoding a fIX variant, wherein the heterologous nucleic acid moleculecomprises or consists of the nucleic acid sequence set forth as SEQ IDNO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 124, or SEQ ID NO: 127,or a nucleic acid sequence at least 90% identical SEQ ID NO: 8, SEQ IDNO: 9, SEQ ID NO: 10, SEQ ID NO: 124, or SEQ ID NO: 127. In several suchembodiments, the recombinant AAV genome (from 5′ to 3′ ITR) is no morethan 5.1, 5.0, 4.9, 4.8, 4.7, 4.6, or 4.5 kb in length.

In some embodiments, a method of inducing blood clotting in a subject inneed thereof is provided. The method comprises administering to thesubject a therapeutically effective amount of a vector (such as an AAVvector) encoding a clotting factor as described herein. In someembodiments, the subject is a subject with a clotting disorder, such ashemophilia A or hemophilia B. In some embodiments, the clotting disorderis hemophilia A and the subject is administered a vector comprising anucleic acid molecule encoding a protein with fVIII activity. In otherembodiments, the clotting disorder is hemophilia B and the subject isadministered a vector comprising a nucleic acid molecule encoding aprotein with fIX activity.

The foregoing and other features and advantages of this disclosure willbecome more apparent from the following detailed description of severalembodiments which proceeds with reference to the accompanying figures.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1A and 1B illustrate a sequence alignment of the A1 and A3 domainsfor human and porcine orthologues of the ET3 variant fVIII protein.(FIG. 1A) Sequence alignment of the A1 domain for human (upper sequence,SEQ ID NO: 13) and porcine (middle sequence, SEQ ID NO: 14) ET3 variantof fVIII. The lower sequence shows identical residues Amino acidsequence alignments for the signal peptide (N-terminal bar), heavy chainacidic domain (C-terminal bar), human (top) and ET3 (bottom) fVIII areshown. Disulfide linkages are noted by the lines connecting cysteineresidues. Places where either human, ET3 or both sequences encode anN-linked glycosylation attachment site (N-X-S/T) are outlined with abox. (FIG. 1B) Sequence alignment of the A3 domain for human (uppersequence, SEQ ID NO: 15) and porcine (middle sequence, SEQ ID NO: 16)ET3 variant of fVIII. The lower sequence shows identical residues Aminoacid sequence alignments for the activation peptide (bar), human (top)and ET3 (bottom) fVIII are shown. Disulfide linkages are noted by thelines connecting cysteine residues. Places where either human, ET3 orboth sequences encode an N-linked glycosylation attachment site(N-X-S/T) are outlined with a box.

FIGS. 2A-2C show liver, total human, and myeloid specific codon biastables.

FIG. 3A shows in vitro expression data in HepG2 cells indicating thatliver specific codon optimization improves expression for the HSQ andET3 variants of the fVIII protein.

FIG. 3B shows in vivo data for codon optimized HSQ and ET3 indicatingincreased expression of fVIII following hydrodynamic injection of anAAV-vector encoding liver codon optimized variants of the HSQ and ET3fVIII protein into mice.

FIG. 4 illustrates AAV vectors encoding fVIII variants.

FIG. 5 shows in vitro expression data in HepG2 cells indicating thatliver specific codon optimization, but not myeloid specific codonoptimization, improves expression of HSQ and ET3 variants of the fVIIIprotein in liver cells.

FIG. 6 shows in vitro expression data in HepG2 cells indicating thatliver specific codon optimization, but not myeloid specific codonoptimization, improves expression of HSQ and ET3 variants of the fVIIIprotein in liver cells.

FIG. 7 shows in vitro expression data in HepG2 cells indicating thatliver specific codon optimization, but not human specific codonoptimization, improves expression of fiX protein in liver cells.

FIG. 8 illustrates promotors comprising an ABP enhancer or a shortenedABP enhancer.

FIGS. 9A and 9B show data concerning use of AAV vectors containing theindicated promoters for expression of fVIII. (FIG. 9A) In vitroexpression data in HepG2 cells. (FIG. 9B) In vivo expression of fVIIIfollowing hydrodynamic injection of an AAV-vector.

FIG. 10 illustrates response element sequences and components of theindicated response elements.

FIGS. 11A and 11B illustrate promotor sequences and components of theindicated promoters.

FIGS. 12A and 12B show data concerning use of AAV vectors containing theindicated promoters for expression of fVIII. (FIG. 12A) In vitroexpression data in HepG2 cells. (FIG. 12B) In vivo expression of fVIIIfollowing hydrodynamic injection of an AAV-vector.

FIG. 13 illustrates promotor sequences and components of the indicatedpromoters.

FIGS. 14A and 14B show data concerning use of AAV vectors containing theindicated promoters for expression of fVIII. (FIG. 14A) In vitroexpression data in HepG2 cells. (FIG. 14B) In vivo expression of fVIIIfollowing hydrodynamic injection of an AAV-vector.

FIGS. 15 and 16 show schematic diagrams illustrating the structure ofliver-specific enhancers (FIG. 15) and promoters including the liverspecific enhancers (FIG. 16).

FIG. 17 shows data from in vitro assays concerning use of AAV vectorscontaining the indicated promoters for expression of fVIII in HepG2cells.

FIG. 18 illustrates an AAV vectors encoding an fVIII variant.

FIG. 19 is a graph showing that transduction of mice with theAAV2-HCB-ET3-LCO-NCG-SpA vector (SEQ ID NO: 130) encoding livercodon-optimized ET3 with deleted CpG motifs leads to a significantincrease in fVIII activity in transduced mice.

SEQUENCE LISTING

The nucleic and amino acid sequences listed in the accompanying sequencelisting are shown using standard letter abbreviations for nucleotidebases, and three letter code for amino acids, as defined in 37 C.F.R.1.822. Only one strand of each nucleic acid sequence is shown, but thecomplementary strand is understood as included by any reference to thedisplayed strand. The Sequence Listing is submitted as an ASCII textfile in the form of the file named “Sequence.txt” (˜148 kb), which wascreated on Dec. 15, 2020, which is incorporated by reference herein.

DETAILED DESCRIPTION

There is a need to develop a safe and efficient gene transfer strategyfor the treatment of hemophilia, such as hemophilia A and B, andacquired hemophilia. In the context of gene therapies for the treatmentof hemophilia A, several obstacles have hindered the development ofusing an adeno-associated viral vector as the gene delivery vehicle,such as the limited DNA packaging capacity of the adeno-associated virusfor the large fVIII transgene, and inefficient biosynthesis of humanfVIII. Reported herein is an AAV-based transgene delivery system thatutilizes improvements for the expression of fVIII in the context ofliver-directed AAV gene transfer. These include: 1) The use a nucleotidecoding sequence that has an improved codon usage bias for the humanliver cell compared to the naturally occurring nucleotide sequence offVIII; 2) Optimization of the codon usage to remove 5′-CG-3′dinucleotides and other deleterious cis-acting DNA motifs, e.g., crypticsplice sites, TATA boxes, terminal signal, mRNA secondary structure,premature polyA signals, RNA instability motifs, internal ribosomalbinding sites; and 3) Minimally sized, liver-directed promoters in orderto reduce the size of the transgene so it may be used in thesize-constrained environment of the adeno-associated viral vectorsystem. The improvements may be generalized for the improved expressionof any AAV transgene. In some embodiments, the AAV vector deliversefficacious expression of fVIII at viral doses not predicted to causetoxicity in humans.

In some embodiments, these improvements may be applied to fiX as well,especially for self-complimentary fiX vector designs. Self-complimentarydesigns have half the packaging capacity is single stranded designs, sovector size limitations (˜2.4 kb) become a concern even for fix.

Prior work suggested that treatment of fVIII-deficient (hemophilia A)mice with an AAV vector encoding a modified form of fVIII (B-domaindeleted) termed ET3 at vector doses ranging from 5×10¹¹-2×10¹³ vp/kgcould theoretically correct their fVIII deficiency and bleedingphenotype (see Brown et al., “Bioengineered Factor FVIII EnablesLong-Term Correction of Murine Hemophilia A Following Liver-DirectedAdeno-Associated Viral Vector Delivery,” Molecular Therapy—Methods andClinical Development. 1:14036, 2014). However, due the oversized genomeof ET3, the vector suffered from low titer manufacture and substantialinter-particle heterogeneity. The large size of the codon optimizedET3-AAV genome remained incompatible with efficient viral vectorpackaging. For AAV vectors, an AAV genome size of no more than 4.7-5.0kb is preferred for higher yield and consistency than genomes exceeding5.0 kb. The B-domain deleted ET3 coding sequence is 4.4 kb. However,with the addition of necessary viral and regulatory control elements,fVIII ET3-AAV genomes substantially exceeded the packaging capacity.

Disclosed herein for the first time is an fVIII (ET3 or other B-domaindeleted variant)-AAV genome of less than 5.0 kb in length that wasdeveloped to allow for both enhanced fVIII (or variant thereof)expression and efficient viral packaging. Multiple steps were taken toreduce the size of the AAV genome to acceptable levels. For example, acombinatorial transcription factor binding site assembly approach wasused to create a panel of liver-specific promoters ranging in size.These promoters represent a 30-90% size reduction over currentlyutilized liver specific promoters such as HLP and HCR-hAAT, which rangein size from 250 to over 700 bases. Some of these promoters drivecomparable or better transgene expression levels and specificity to thatobserved with HLP and HCR-hAAT.

A significant barrier to the development of successful clinical genetransfer-based therapeutics is the availability of naturally occurringor synthetic genetic elements capable of functional, and often celltype-directed or restricted, expression in the context of avector-delivered nucleic acid cassette (see, e.g., Papadakis et al.,“Promoters and control elements: designing expression cassettes for genetherapy,” Curr Gene Ther., 4(1):89-113, 2004). It is generally believedthat naturally existing promoters have been honed by evolution to drivefinely tuned expression through the combination of multiplecis-regulatory sequences. In most living organisms, and especiallyeukaryotes with large genome sizes, there does not appear to be adriving force to limit promoter size and thus most endogenous promotesare spread over hundreds, and more often thousands, of DNA basepairs(bp). Due to their size, these endogenous, native gene promoterstypically are not amenable to inclusion into gene therapy products dueto size constraints.

Endogenous viral promoters on the other hand have evolved to possess anefficiency of strength and size than make them attractive for use ingene transfer technologies. Prominent examples include thecytomegalovirus (CMV) immediate early (IE) promoter, the adenovirus (Ad)major late promoter, simian virus 40 (SV40) promoter and Moloney murineleukemia virus (MoMLV) long terminal repeat (LTR). Each of thesepromoters can drive high-level transcription of exogenous heterologoustransgenes in a variety of eukaryotic cell types. However, notsurprisingly, eukaryotic cells have developed cellular defensemechanisms to effectively detect and inactivate (i.e. silence) viralpromoters and thus these promoters perform more effectively in cellculture model systems than in vivo gene therapy applications.

For these reasons, there has been significant interest in thedevelopment of synthetic promoters, either generic (see, e.g.,Juven-Gershon et al., “Rational design of a super core promoter thatenhances gene expression,” Nat Methods, 3(11):917-22, 2006; Schlabach etal., “Synthetic design of strong promoters.” PNAS, 2010; 107(6):2538-43,2010), or tailored to specific gene therapy applications includinghemophilia A and B (see, e.g., McIntosh et al., “Therapeutic levels ofFVIII following a single peripheral vein administration of rAAV vectorencoding a novel human factor VIII variant,” Blood, 121(17):3335-44,2013; Nair et al., “Computationally designed liver-specifictranscriptional modules and hyperactive factor IX improve hepatic genetherapy,” Blood, 123(20):3195-9, 2014).

Knowledge of promoters and enhances remains limited and currently it isnot possible to computationally design an optimal promoter with anyconfidence. Studies such as those described by Juven-Gershon andKadonaga have made progress defining optimized core promoter designssuch as their Super Core Promoter 1 (SCP1) and are informative to thefield. However, as we show in promoters described in the examplesherein, which do not contain strong similarity to SCP1 in the corepromoter domain, these sequences are not necessary for strong promoterfunction, at least in the context of liver-directed gene therapyapplications (see also, Juven-Gershon et al., “Rational design of asuper core promoter that enhances gene expression,” Nat Methods,3(11):917-22, 2006).

Most generic promoter development has focused on achieving an optimalbalance of transcriptional potency with minimal size. In the field ofliver-directed promoter design, the use of rational design approaches byMcIntosh et al. and Nair et al. (supra) led to identification ofpromoters for use in AAV-fVIII and AAV-fIX gene therapy approaches.However despite extensive study, both groups describe promoter designsthat are significantly larger (>252 bp) and no more (or less) potentthan those described herein such as SEQ ID NO: 4 (HCB). Indeed, giventhe prior attempts to optimize promoter design, it was particularlysurprising to identify promoters such as those described herein that aresmaller that prior art promoters (such as the HLP promoter), yetequivalent or enhanced potency for driving transcription, particularlyin the context of in vivo gene therapy applications.

I. Terms

Unless otherwise noted, technical terms are used according toconventional usage. Definitions of common terms in molecular biology maybe found in Benjamin Lewin, Genes V, published by Oxford UniversityPress, 1994 (ISBN 0-19-854287-9); Kendrew et al. (eds.), TheEncyclopedia of Molecular Biology, published by Blackwell Science Ltd.,1994 (ISBN 0-632-02182-9); and Robert A. Meyers (ed.), Molecular Biologyand Biotechnology: a Comprehensive Desk Reference, published by VCHPublishers, Inc., 1995 (ISBN 1-56081-569-8).

In order to facilitate review of the various embodiments of thedisclosure, the following explanations of specific terms are provided:

5′ and/or 3′: Nucleic acid molecules (such as, DNA and RNA) are said tohave “5′ ends” and “3′ ends” because mononucleotides are reacted to makepolynucleotides in a manner such that the 5′ phosphate of onemononucleotide pentose ring is attached to the 3′ oxygen of its neighborin one direction via a phosphodiester linkage. Therefore, one end of alinear polynucleotide is referred to as the “5′ end” when its 5′phosphate is not linked to the 3′ oxygen of a mononucleotide pentosering. The other end of a polynucleotide is referred to as the “3′ end”when its 3′ oxygen is not linked to a 5′ phosphate of anothermononucleotide pentose ring. Notwithstanding that a 5′ phosphate of onemononucleotide pentose ring is attached to the 3′ oxygen of itsneighbor, an internal nucleic acid sequence also may be said to have 5′and 3′ ends.

In either a linear or circular nucleic acid molecule, discrete internalelements are referred to as being “upstream” or 5′ of the “downstream”or 3′ elements. With regard to DNA, this terminology reflects thattranscription proceeds in a 5′ to 3′ direction along a DNA strand.Promoter and enhancer elements, which direct transcription of a linkedgene, are generally located 5′ or upstream of the coding region.However, enhancer elements can exert their effect even when located 3′of the promoter element and the coding region. Transcription terminationand polyadenylation signals are located 3′ or downstream of the codingregion.

Adeno-associated virus (AAV): A small, replication-defective,non-enveloped virus that infects humans and some other primate species.AAV is not known to cause disease and elicits a very mild immuneresponse. Gene therapy vectors that utilize AAV can infect both dividingand quiescent cells and can persist in an extrachromosomal state withoutintegrating into the genome of the host cell. These features make AAV anattractive viral vector for gene therapy. There are currently 11recognized serotypes of AAV (AAV1-11).

Administration/Administer: To provide or give a subject an agent, suchas a therapeutic agent (e.g. a recombinant AAV), by any effective route.Exemplary routes of administration include, but are not limited to,injection (such as subcutaneous, intramuscular, intradermal,intraperitoneal, and intravenous), oral, intraductal, sublingual,rectal, transdermal, intranasal, vaginal and inhalation routes.

Bleeding Time Assay: An assay used to measure the amount of time ittakes for a subject's blood to clot. A blood pressure cuff is placed onthe upper arm and inflated. Two incisions are made on the lower arm.These are about 10 mm (less than ½ inch) long and 1 mm deep (just deepenough to cause minimal bleeding). The blood pressure cuff isimmediately deflated. Blotting paper is touched to the cuts every 30seconds until the bleeding stops. The length of time it takes for thecuts to stop bleeding is recorded. In normal, non-hemophiliacs, bleedingstops within about one to ten minutes and may vary from lab to lab,depending on how the assay is measured. In contrast, severe hemophiliacshaving less than 1% of normal levels of the appropriate clotting factorhave a whole blood clotting time of greater than 60 minutes. In mice,the bleeding time is assayed by transecting the tip of the tail andperiodically touching a blotting paper until a clot is formed at the tipof the tail. Normal bleeding time is between 2-4 minutes. In contrast,hemophiliac mice having less than 1% of normal levels of the appropriateclotting factor have a bleeding time of greater than 15 minutes.

cDNA (complementary DNA): A piece of DNA lacking internal, non-codingsegments (introns) and regulatory sequences that determinetranscription. cDNA is synthesized in the laboratory by reversetranscription from messenger RNA extracted from cells. cDNA can alsocontain untranslated regions (UTRs) that are responsible fortranslational control in the corresponding RNA molecule.

Clotting disorder: A general term for a wide range of medical problemsthat lead to poor blood clotting and continuous bleeding. Doctors alsorefer to clotting disorders by terms such as, for example, coagulopathy,abnormal bleeding and bleeding disorders. Clotting disorders include anycongenital, acquired or induced defect that results in abnormal (orpathological) bleeding. Examples include, but are not limited to,disorders of insufficient clotting or hemostasis, such as hemophilia A(a deficiency in fVIII), hemophilia B (a deficiency in fix), hemophiliaC (a deficiency in Factor XI), other clotting factor deficiencies (suchas Factor VII or fXIII), abnormal levels of clotting factor inhibitors,platelet disorders, thrombocytopenia, vitamin K deficiency and vonWillebrand's disease.

Some clotting disorders are present at birth and in some instances areinherited disorders. Specific examples include, but are not limited to:hemophilia A, hemophilia B, protein C deficiency, and Von Willebrand'sdisease. Some clotting disorders are developed during certain illnesses(such as vitamin K deficiency, severe liver disease), or treatments(such as use of anticoagulant drugs or prolonged use of antibiotics).

Clotting factor: Includes any protein which promotes proper hemostasis.In one embodiment, a clotting factor is fVIII or flX, or a variant orfragment thereof which retains its hemostatic activity, for example asmeasured using an APTT assay or a bleeding time assay. In someembodiments, when administered in a therapeutically effective amount,the clotting factor increases hemostasis in a subject suffering from aclotting disorder, such as hemophilia.

Clotting Factor VIII (fVIII): fVIII is a protein required for theefficient clotting of blood, and functions in coagulation as a cofactorin the activation of factor X by fix. A concentration of about 100 ng/mlfor fVIII in the blood is considered in the normal range. Deficiency offVIII is associated with hemophilia A, and severe forms of the diseasecan result when a subject has less than about 1% of the normal amount offVIII (i.e. less than about 1 ng of fVIII per ml of blood). fVIII issynthesized as a 2351 amino acid single chain precursor protein, whichis proteolytically processed. The human factor VIII gene (186,000base-pairs) consists of 26 exons ranging in size from 69 to 3,106 bp andintrons as large as 32.4 kilobases (kb). Examples of fVIII nucleic acidand protein sequences are publicly available (for example, see GenbankAccession Nos: K01740, M14113, and E00527). fVIII variants are providedherein that retain fVIII activity for blood clotting but are reduced insize, such as fVIII variants that lack the fVIII B domain. ExemplaryfVIII variants include the HSQ and ET3 variants.

Clotting Factor IX (fIX): fIX is a vitamin K-dependent protein requiredfor the efficient clotting of blood, and functions in coagulation as anactivator of factor X. A concentration of about 1-5 μg/ml of fiX in theblood is considered in the normal range. Deficiency of fiX is associatedwith hemophilia B, and severe cases result when the concentration of fIXis less than about 1% of the normal concentration of fiX (i.e. less thanabout 0.01-0.05 μg fiX per ml of blood). fX nucleic acid and proteinsequences are publicly available (for example see Kurachi et al., 1982.Proc. Natl. Acad. Sci. U.S.A. 79(21):6461-4; Genbank Accession Nos:J00136, XM045316, K02402, J00137, and M11309.

Codon-optimized: A “codon-optimized” nucleic acid refers to a nucleicacid sequence that has been altered such that the codons are optimal forexpression in a particular system (such as a particular species or groupof species). For example, a nucleic acid sequence can be optimized forexpression in mammalian cells or in a particular mammalian species (suchas human cells). Codon optimization does not alter the amino acidsequence of the encoded protein.

The term “liver specific amino acids codons” refers to codons that aredifferentially utilized-represented in genes highly expressed within thehuman liver compared to the codon usage of the entire coding region ofthe human genome. A strategy using a maximum amount of liver specificamino acid codons seeks to avoid codons that are under-represented,e.g., because of low quantities of codon matching tRNA in liver cellsresulting in slower protein translation.

Control: A reference standard. In some embodiments, the control is anegative control sample obtained from a healthy patient. In otherembodiments, the control is a positive control sample obtained from apatient diagnosed with hemophilia. In still other embodiments, thecontrol is a historical control or standard reference value or range ofvalues (such as a previously tested control sample, such as a group ofhemophilia A patients with known prognosis or outcome, or group ofsamples that represent baseline or normal values).

A difference between a test sample and a control can be an increase orconversely a decrease. The difference can be a qualitative difference ora quantitative difference, for example a statistically significantdifference. In some examples, a difference is an increase or decrease,relative to a control, of at least about 5%, such as at least about 10%,at least about 20%, at least about 30%, at least about 40%, at leastabout 50%, at least about 60%, at least about 70%, at least about 80%,at least about 90%, at least about 100%, at least about 150%, at leastabout 200%, at least about 250%, at least about 300%, at least about350%, at least about 400%, at least about 500%, or greater than 500%.

DNA (deoxyribonucleic acid): DNA is a long chain polymer which comprisesthe genetic material of most living organisms (some viruses have genescomprising ribonucleic acid (RNA)). The repeating units in DNA polymersare four different nucleotides, each of which comprises one of the fourbases, adenine (A), guanine (G), cytosine (C), and thymine (T) bound toa deoxyribose sugar to which a phosphate group is attached. Triplets ofnucleotides (referred to as codons) code for each amino acid in apolypeptide, or for a stop signal. The term codon is also used for thecorresponding (and complementary) sequences of three nucleotides in themRNA into which the DNA sequence is transcribed.

Unless otherwise specified, any reference to a DNA molecule is intendedto include the reverse complement of that DNA molecule. Except wheresingle-strandedness is required by the text herein, DNA molecules,though written to depict only a single strand, encompass both strands ofa double-stranded DNA molecule. Thus, a reference to the nucleic acidmolecule that encodes a specific protein, or a fragment thereof,encompasses both the sense strand and its reverse complement. Forinstance, it is appropriate to generate probes or primers from thereverse complement sequence of the disclosed nucleic acid molecules.

Enhancer: A nucleic acid sequence that increases the rate oftranscription by increasing the activity of a promoter.

Flanking: Near or next to, also, including adjoining, for instance in alinear or circular polynucleotide, such as a DNA molecule.

Gene: A nucleic acid sequence, typically a DNA sequence, that comprisescontrol and coding sequences necessary for the transcription of an RNA,whether an mRNA or otherwise. For instance, a gene may comprise apromoter, one or more enhancers or silencers, a nucleic acid sequencethat encodes a RNA and/or a polypeptide, downstream regulatory sequencesand, possibly, other nucleic acid sequences involved in regulation ofthe expression of an mRNA.

As is well known in the art, most eukaryotic genes contain both exonsand introns. The term “exon” refers to a nucleic acid sequence found ingenomic DNA that is bioinformatically predicted and/or experimentallyconfirmed to contribute a contiguous sequence to a mature mRNAtranscript. The term “intron” refers to a nucleic acid sequence found ingenomic DNA that is predicted and/or confirmed not to contribute to amature mRNA transcript, but rather to be “spliced out” during processingof the transcript.

Gene therapy: The introduction of a heterologous nucleic acid moleculeinto one or more recipient cells, wherein expression of the heterologousnucleic acid in the recipient cell affects the cell's function andresults in a therapeutic effect in a subject. For example, theheterologous nucleic acid molecule may encode a protein, which affects afunction of the recipient cell.

Hemophilia: A blood coagulation disorder caused by a deficient clottingfactor activity, which decreases hemostasis. Severe forms result whenthe concentration of clotting factor is less than about 1% of the normalconcentration of the clotting factor in a normal subject. In somesubjects, hemophilia is due to a genetic mutation which results inimpaired expression of a clotting factor. In others, hemophilia is anauto-immune disorder, referred to as acquired hemophilia, in which theantibodies which are generated against a clotting factor in a subjectresult in decreased hemostasis.

Hemophilia A results from a deficiency of functional clotting fVIII,while hemophilia B results from a deficiency of functional clotting fix.These conditions which are due to a genetic mutation are caused by aninherited sex-linked recessive trait with the defective gene located onthe X chromosome, and this disease is therefore generally found only inmales. The severity of symptoms can vary with this disease, and thesevere forms become apparent early on. Bleeding is the hallmark of thedisease and typically occurs when a male infant is circumcised.Additional bleeding manifestations make their appearance when the infantbecomes mobile. Mild cases may go unnoticed until later in life whenthey occur in response to surgery or trauma. Internal bleeding mayhappen anywhere, and bleeding into joints is common.

Hemostasis: Arrest of bleeding blood by blood clot formation. Bloodclotting time is the length of time it takes for peripheral blood toclot using an activated partial thromboplastin time assay (APTT) or bymeasuring bleeding time. In a particular embodiment, the blood clottingtime decreases by at least 50%, for example at least 60%, at least 70%,at least 75%, at least 80%, at least 90%, at least 95%, at least 98%, atleast 99% or even about 100% (i.e. the blood clotting time is similar towhat is observed for a normal subject) when compared to the bloodclotting time of the subject prior to administration of a therapeuticvector encoding the appropriate clotting factor as described herein. Inyet another embodiment, the blood clotting time in the affected subjectis corrected to about 50% of a normal subject, to about 75% of a normalsubject, to about 90% of a normal subject, for example to about 95%, forexample about 100%, after oral administration of a therapeuticallyeffective amount of the appropriate clotting factor. As used herein,“about” refers to plus or minus 5% from a reference value. Thus, about50% refers to 47.5% to 52.5%.

Intron: A stretch of DNA within a gene that does not contain codinginformation for a protein.

Introns are removed before translation of a messenger RNA.

Inverted terminal repeat (ITR): Symmetrical nucleic acid sequences inthe genome of adeno-associated viruses required for efficientreplication. ITR sequences are located at each end of the AAV DNAgenome. The ITRs serve as the origins of replication for viral DNAsynthesis and are essential cis components for generating AAVintegrating vectors.

Isolated: An “isolated” biological component (such as a nucleic acidmolecule, protein, virus or cell) has been substantially separated orpurified away from other biological components in the cell or tissue ofthe organism, or the organism itself, in which the component naturallyoccurs, such as other chromosomal and extra-chromosomal DNA and RNA,proteins and cells. Nucleic acid molecules and proteins that have been“isolated” include those purified by standard purification methods. Theterm also embraces nucleic acid molecules and proteins prepared byrecombinant expression in a host cell as well as chemically synthesizednucleic acid molecules and proteins.

Nucleic acid molecule: A polymeric form of nucleotides, which mayinclude both sense and anti-sense strands of RNA, cDNA, genomic DNA, andsynthetic forms and mixed polymers of the above. A nucleotide refers toa ribonucleotide, deoxynucleotide or a modified form of either type ofnucleotide. The term “nucleic acid molecule” as used herein issynonymous with “nucleic acid” and “polynucleotide.” A nucleic acidmolecule is usually at least 10 bases in length, unless otherwisespecified. The term includes single- and double-stranded forms of DNA. Apolynucleotide may include either or both naturally occurring andmodified nucleotides linked together by naturally occurring and/ornon-naturally occurring nucleotide linkages. “cDNA” refers to a DNA thatis complementary or identical to an mRNA, in either single stranded ordouble stranded form. “Encoding” refers to the inherent property ofspecific sequences of nucleotides in a polynucleotide, such as a gene, acDNA, or an mRNA, to serve as templates for synthesis of other polymersand macromolecules in biological processes having either a definedsequence of nucleotides (i.e., rRNA, tRNA and mRNA) or a definedsequence of amino acids and the biological properties resultingtherefrom.

Nucleotide: This term includes, but is not limited to, a monomer thatincludes a base linked to a sugar, such as a pyrimidine, purine orsynthetic analogs thereof, or a base linked to an amino acid, as in apeptide nucleic acid (PNA). A nucleotide is one monomer in apolynucleotide. A nucleotide sequence refers to the sequence of bases ina polynucleotide.

Operably linked: A first nucleic acid sequence is operably linked with asecond nucleic acid sequence when the first nucleic acid sequence isplaced in a functional relationship with the second nucleic acidsequence. For instance, a promoter is operably linked to a codingsequence if the promoter affects the transcription or expression of thecoding sequence. Generally, operably linked DNA sequences are contiguousand, where necessary to join two protein-coding regions, in the samereading frame.

ORF (open reading frame): A series of nucleotide triplets (codons)coding for amino acids. These sequences are usually translatable into apeptide.

Pharmaceutically acceptable carriers: The pharmaceutically acceptablecarriers of use are conventional. Remington's Pharmaceutical Sciences,by E. W. Martin, Mack Publishing Co., Easton, Pa., 19th Edition, 1995,describes compositions and formulations suitable for pharmaceuticaldelivery of the disclosed vectors.

In general, the nature of the carrier will depend on the particular modeof administration being employed. For instance, parenteral formulationsusually comprise injectable fluids that include pharmaceutically andphysiologically acceptable fluids such as water, physiological saline,balanced salt solutions, aqueous dextrose, glycerol or the like as avehicle. For solid compositions (e.g., powder, pill, tablet, or capsuleforms), conventional non-toxic solid carriers can include, for example,pharmaceutical grades of mannitol, lactose, starch, or magnesiumstearate. In addition to biologically neutral carriers, pharmaceuticalcompositions (such as vector compositions) to be administered cancontain minor amounts of non-toxic auxiliary substances, such as wettingor emulsifying agents, preservatives, and pH buffering agents and thelike, for example sodium acetate or sorbitan monolaurate. In particularembodiments, suitable for administration to a subject the carrier may besterile, and/or suspended or otherwise contained in a unit dosage formcontaining one or more measured doses of the composition suitable toinduce the desired immune response. It may also be accompanied bymedications for its use for treatment purposes. The unit dosage form maybe, for example, in a sealed vial that contains sterile contents or asyringe for injection into a subject, or lyophilized for subsequentsolubilization and administration or in a solid or controlled releasedosage.

Polypeptide: Any chain of amino acids, regardless of length orpost-translational modification (e.g., glycosylation orphosphorylation). “Polypeptide” applies to amino acid polymers includingnaturally occurring amino acid polymers and non-naturally occurringamino acid polymer as well as in which one or more amino acid residue isa non-natural amino acid, for example, an artificial chemical mimetic ofa corresponding naturally occurring amino acid. A “residue” refers to anamino acid or amino acid mimetic incorporated in a polypeptide by anamide bond or amide bond mimetic. A polypeptide has an amino terminal(N-terminal) end and a carboxy terminal (C-terminal) end. “Polypeptide”is used interchangeably with peptide or protein, and is used herein torefer to a polymer of amino acid residues.

Preventing, treating or ameliorating a disease: “Preventing” a disease(such as hemophilia) refers to inhibiting the full development of adisease. “Treating” refers to a therapeutic intervention thatameliorates a sign or symptom of a disease or pathological conditionafter it has begun to develop. “Ameliorating” refers to the reduction inthe number or severity of signs or symptoms of a disease.

Promoter: A region of DNA that directs/initiates transcription of anucleic acid (e.g. a gene). A promoter includes necessary nucleic acidsequences near the start site of transcription. Typically, promoters arelocated near the genes they transcribe. A promoter also optionallyincludes distal enhancer or repressor elements which can be located asmuch as several thousand base pairs from the start site oftranscription. A tissue-specific promoter is a promoter thatdirects/initiated transcription primarily in a single type of tissue orcell. For example, a liver-specific promoter is a promoter thatdirects/initiates transcription in liver tissue to a substantiallygreater extent than other tissue types.

Protein: A biological molecule expressed by a gene or other encodingnucleic acid (e.g., a cDNA) and comprised of amino acids.

Purified: The term “purified” does not require absolute purity; rather,it is intended as a relative term. Thus, for example, a purifiedpeptide, protein, virus, or other active compound is one that isisolated in whole or in part from naturally associated proteins andother contaminants. In certain embodiments, the term “substantiallypurified” refers to a peptide, protein, virus or other active compoundthat has been isolated from a cell, cell culture medium, or other crudepreparation and subjected to fractionation to remove various componentsof the initial preparation, such as proteins, cellular debris, and othercomponents.

Recombinant: A recombinant nucleic acid molecule is one that has asequence that is not naturally occurring, for example, includes one ormore nucleic acid substitutions, deletions or insertions, and/or has asequence that is made by an artificial combination of two otherwiseseparated segments of sequence. This artificial combination can beaccomplished by chemical synthesis or, more commonly, by the artificialmanipulation of isolated segments of nucleic acids, for example, bygenetic engineering techniques.

A recombinant virus is one that includes a genome that includes arecombinant nucleic acid molecule. As used herein, “recombinant AAV”refers to an AAV particle in which a recombinant nucleic acid molecule(such as a recombinant nucleic acid molecule encoding a clotting factor)has been packaged.

A recombinant protein is one that has a sequence that is not naturallyoccurring or has a sequence that is made by an artificial combination oftwo otherwise separated segments of sequence. In several embodiments, arecombinant protein is encoded by a heterologous (for example,recombinant) nucleic acid that has been introduced into a host cell,such as a bacterial or eukaryotic cell, or into the genome of arecombinant virus.

Response element (RE): A DNA sequence included in a promoter to whichone or more transcription factors can bind to and confer an aspect ofcontrol of gene expression.

Sequence identity: The identity or similarity between two or morenucleic acid sequences, or two or more amino acid sequences, isexpressed in terms of the identity or similarity between the sequences.Sequence identity can be measured in terms of percentage identity; thehigher the percentage, the more identical the sequences are. Sequencesimilarity can be measured in terms of percentage similarity (whichtakes into account conservative amino acid substitutions); the higherthe percentage, the more similar the sequences are. Homologs ororthologs of nucleic acid or amino acid sequences possess a relativelyhigh degree of sequence identity/similarity when aligned using standardmethods. This homology is more significant when the orthologous proteinsor cDNAs are derived from species which are more closely related (suchas human and mouse sequences), compared to species more distantlyrelated (such as human and C. elegans sequences).

Methods of alignment of sequences for comparison are well known in theart. Various programs and alignment algorithms are described in: Smith &Waterman, Adv. Appl. Math. 2:482, 1981; Needleman & Wunsch, J. Mol.Biol. 48:443, 1970; Pearson & Lipman, Proc. Natl. Acad. Sci. USA85:2444, 1988; Higgins & Sharp, Gene, 73:237-44, 1988; Higgins & Sharp,CABIOS 5:151-3, 1989; Corpet et al., Nuc. Acids Res. 16:10881-90, 1988;Huang et al. Computer Appls. in the Biosciences 8, 155-65, 1992; andPearson et al., Meth. Mol. Bio. 24:307-31, 1994. Altschul et al., J.Mol. Biol. 215:403-10, 1990, presents a detailed consideration ofsequence alignment methods and homology calculations.

The NCBI Basic Local Alignment Search Tool (BLAST) (Altschul et al., J.Mol. Biol. 215:403-10, 1990) is available from several sources,including the National Center for Biological Information (NCBI) and onthe internet, for use in connection with the sequence analysis programsblastp, blastn, blastx, tblastn and tblastx. Additional information canbe found at the NCBI web site.

As used herein, reference to “at least 90% identity” refers to “at least90%, at least 91%, at least 92%, at least 93%, at least 94%, at least95%, at least 96%, at least 97%, at least 98%, at least 99%, or even100% identity” to a specified reference sequence.

Subject: Living multi-cellular vertebrate organisms, a category thatincludes human and non-human mammals

Synthetic: Produced by artificial means in a laboratory, for example asynthetic nucleic acid can be chemically synthesized in a laboratory.

TATA box: A DNA sequence found in the promoter region of a gene that canbe bound by TATA binding protein and transcription factor II D duringDNA unwinding and binding by RNA polymerase II. A TATA box sequencetypically includes a TATAAA sequence and often includes additional 3′adenine nucleotides. An exemplary TATA box sequence is provided asnucleotides 108-114 of SEQ ID NO: 4.

Therapeutically effective amount: A quantity of a specifiedpharmaceutical or therapeutic agent (e.g. a recombinant AAV) sufficientto achieve a desired effect in a subject, or in a cell, being treatedwith the agent. The effective amount of the agent will be dependent onseveral factors, including, but not limited to the subject or cellsbeing treated, and the manner of administration of the therapeuticcomposition.

Transcription factor (TF): A protein that binds to specific DNAsequences and thereby controls the transfer (or transcription) ofgenetic information from DNA to RNA. IFs perform this function alone orwith other proteins in a complex, by promoting (as an activator), orblocking (as a repressor) the recruitment of RNA polymerase (the enzymethat performs the transcription of genetic information from DNA to RNA)to specific genes. The specific DNA sequences to which a TF hinds isknown as a response element (RE) or regulatory element. Other namesinclude cis-element and cis-acting transcriptional regulatory element.

Transcription factors interact with their binding sites using acombination of electrostatic (of which hydrogen bonds are a specialcase) and Van der Waals forces. Due to the nature of these chemicalinteractions, most transcription factors bind DNA in a sequence specificmanner. However, not all bases in the transcription factor-binding sitemay actually interact with the transcription factor. In addition, someof these interactions may be weaker than others. Thus, manytranscription factors do not bind just one sequence but are capable ofbinding a subset of closely related sequences, each with a differentstrength of interaction.

For example, although the consensus binding site for the TATA-bindingprotein (TBP) is TATAAAA; however, the TBP transcription factor can alsobind similar sequences such as TATATAT or TATATAA,

Transcription factors (TFs) are classified based on many aspects. Forexample, the secondary, tertiary and quaternary structures of theprotein structures DNA-binding sequence and properties, the interactionwith the double helix of the DNA, and the metal and other bindingcharacteristics. The JASPAR database and TRANSFAC (TRANSFAC® 7.0 Public2005) are two web-based transcription factor databases, theirexperimentally-proven binding sites, and regulated genes.

-   -   HNF1a: Also called HNF1 Homeobox A or HNF1, the HNF1a protein is        a transcription factor required for the expression of several        liver specific genes. HNF1a forms a homodimer that binds to        particular promoter sequences. Exemplary HNF1a TF binding sites        include the “HNF1a” TF binding site provided as nucleotides 1-12        of SEQ ID NO: 4, the “HNF1-1” TF binding site provided as        nucleotides 16-23 of SEQ ID NO: 4, and the “HNF1-2” TF binding        site provided as nucleotides 48-62 of SEQ ID NO: 4. (See, e.g.,        PubMed Gene ID NO. 6927; Chi et al., “Diabetes mutations        delineate an atypical POU domain in HNF-1alpha,” Mol. Cell.,        10:1129-1137, 2002; and Rose et al., “Structural basis of        dimerization, coactivator recognition and MODY3 mutations in        HNF-1alpha,” Nat. Struct. Biol. 7:744-748, 2000).    -   HNF3a: A transcription factor required for the expression of        several liver specific genes. HNF3a binds to particular promoter        sequences. An exemplary HNF3a TF binding site is provided as        nucleotides 39-45 of SEQ ID NO: 4. An exemplary HNF3-2 TF        binding site is provided as nucleotides 65-71 of SEQ ID NO: 4.        (see, e.g., Laganiere et al., “Location analysis of estrogen        receptor alpha target promoters reveals that FOXA1 defines a        domain of the estrogen response,” Proc. Natl. Acad. Sci. U.S.A.        102:11651-11656, 2005; Williamson et al., “BRCA1 and FOXA1        proteins coregulate the expression of the cell cycle-dependent        kinase inhibitor p27(Kip1),” Oncogene 25:1391-1399, 2006; Lupien        et al., “FoxA1 translates epigenetic signatures into        enhancer-driven lineage-specific transcription,” Cell        132:958-970, 2008; Song et al., “Role of FoxA1 in regulation of        bcl2 expression during oxidative-stress-induced apoptosis in        A549 type II pneumocytes,” Cell Stress Chaperones, 14:417-425,        2009); and Malik et al., “Histone deacetylase 7 and FoxA1 in        estrogen-mediated repression of RPRM,” Mol. Cell. Biol.        30:399-412, 2010).    -   HNF4: A transcription factor required for the expression of        several liver specific genes. HNF4 binds to particular promoter        sequences. An exemplary HNF4 TF binding site is provided as        nucleotides 26-36 of SEQ ID NO: 4. (See, e.g., Wang et al.,        “Hepatocyte nuclear factor-4a interacts with other hepatocyte        nuclear factors in regulating transthyretin gene expression,”        FEBS J., 277(19):4066-75, 2010).    -   HP1: A transcription factor required for the expression of        several liver specific genes. HP1 binds to particular promoter        sequences. An exemplary HP1 TF binding site is provided as        nucleotides 75-87 of SEQ ID NO: 4. (See, e.g., Schorpp et al.,        “Hepatocyte-specific promoter element HP1 of the Xenopus albumin        gene interacts with transcriptional factors of mammalian        hepatocytes,” J Mol Biol., 202(2):307-20, 1988)

Transcription Start Site: The location where transcription starts at the5′ end of a gene sequence. An exemplary Transcription Start Site isprovided as nucleotides 116-146 of SEQ ID NO: 4.

Therapeutically effective amount: The amount of agent, such as adisclosed recombinant AAV vector encoding a clotting factor, that issufficient to prevent, treat (including prophylaxis), reduce and/orameliorate the symptoms and/or underlying causes of a disorder ordisease, for example to prevent, inhibit, and/or treat hemophilia. Forinstance, this can be the amount necessary to inhibit or prevent viralreplication or to measurably alter outward symptoms of the disease orcondition.

In one example, a desired response is to reduce clotting time in asubject (such as a subject with hemophilia), for example as measuredusing a bleeding time assay. The clotting time does not need to becompletely restored to that of normal healthy subjects withouthemophilia for the method to be effective. For example, administrationof a therapeutically effective amount of a vector (such as a fVIIIencoding vector) as disclosed herein can decrease the clotting time (orother symptom of the hemophilia) by a desired amount, for example by atleast 20%, at least 30%, at least 40%, at least 50%, at least 60%, atleast 70%, at least 80%, at least 90%, at least 95%, at least 98%, atleast 100% or more, as compared to a suitable control.

It is understood that to obtain a therapeutic response to the disease orcondition can require multiple administrations of the agent. Thus, atherapeutically effective amount encompasses a fractional dose thatcontributes in combination with previous or subsequent administrationsto attaining a therapeutic outcome in the patient. For example, atherapeutically effective amount of an agent can be administered in asingle dose, or in several doses, for example daily, during a course oftreatment. However, the therapeutically effective amount can depend onthe subject being treated, the severity and type of the condition beingtreated, and the manner of administration. A unit dosage form of theagent can be packaged in a therapeutic amount, or in multiples of thetherapeutic amount, for example, in a vial (e.g., with a pierceable lid)or syringe having sterile components.

Vector: A vector is a nucleic acid molecule allowing insertion offoreign nucleic acid without disrupting the ability of the vector toreplicate and/or integrate in a host cell. A vector can include nucleicacid sequences that permit it to replicate in a host cell, such as anorigin of replication. A vector can also include one or more selectablemarker genes and other genetic elements. An expression vector is avector that contains the necessary regulatory sequences to allowtranscription and translation of inserted gene or genes. In someembodiments herein, the vector is an adeno-associated virus (AAV)vector. In some embodiments, the vector is a gamma-retroviral vector, alentiviral vector, or an adenoviral vector.

Unless otherwise explained, all technical and scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which this disclosure belongs. The singular terms“a,” “an,” and “the” include plural referents unless context clearlyindicates otherwise. “Comprising A or B” means including A, or B, or Aand B. It is further to be understood that all base sizes or amino acidsizes, and all molecular weight or molecular mass values, given fornucleic acids or polypeptides are approximate, and are provided fordescription. Although methods and materials similar or equivalent tothose described herein can be used in the practice or testing of thepresent disclosure, suitable methods and materials are described below.All publications, patent applications, patents, and other referencesmentioned herein are incorporated by reference in their entirety. Incase of conflict, the present specification, including explanations ofterms, will control. In addition, the materials, methods, and examplesare illustrative only and not intended to be limiting.

II. Optimized Promotors for Liver-Directed Transcription

Novel promoters are provided herein for promoting transcription in livertissue and/or cells. As discussed in Example 2, the new promoters weredesigned using an iterative approach that ultimately identified severalpromoter sequences that provide unexpectedly high transcription levels(as assayed by measuring expressed protein activity), and aresubstantially shorter than prior promoter sequences, such as the HLPpromoter sequence.

In some embodiments, a recombinant nucleic acid molecule is providedthat comprises a promoter comprising a first response element comprisesa set of transcription factor (TF) binding sites, including: a HNF1a TFbinding site, a HNF1-1 TF binding site, a HNF4 TF binding site, a HNF3aTF binding site, a HNF1-2 TF binding site, a HNF3-2 TF binding site, aHP1 TF binding site, a TATA box; and a Transcription Start Site. Theseare the transcription factor binding sites included on the HCB promoter.

In some embodiments, the first response element can comprise anucleotide sequence that is no more than 160 nucleotides in length (suchas no more than 150 nucleotides in length, such as 146 nucleotides inlength).

In some embodiments, the HNF1a TF binding site comprises or consists ofnucleotides 1-12 of SEQ ID NO: 4; the HNF1-1 TF binding site comprisesor consists of nucleotides 16-23 of SEQ ID NO: 4; the HNF4 TF bindingsite comprises or consists of nucleotides 26-36 of SEQ ID NO: 4; theHNF3a TF binding site comprises or consists of nucleotides 39-45 of SEQID NO: 4; the HNF1-2 TF binding site comprises or consists ofnucleotides 48-62 of SEQ ID NO: 4; the HNF3-2 TF binding site comprisesor consists of nucleotides 65-71 of SEQ ID NO: 4; the HP1 TF bindingsite comprises or consists of nucleotides 75-87 of SEQ ID NO: 4; theTATA box comprises or consists of nucleotides 108-114 of SEQ ID NO: 4;and/or the Transcription Start Site (TSS) comprises or consists ofnucleotides 116-146 of SEQ ID NO: 4.

In some embodiments, the first response element comprises, from 5′ to3′, the HNF1a TF binding site, the HNF1-1 TF binding site, the HNF-4 TFbinding site, the HNF3a TF binding site, the HNF1-2 TF binding site, theHNF3-2 TF binding site, the HP1 TF binding site, the TATA box, and theTranscription Start Site (TSS).

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 4 (HCB), or a sequence at least 90% (such as at least 91%,at least 92%, at least 93%, at least 94%, at least 95%, at least 98%, orat least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule can comprisea promoter comprising the first response element as discussed above, andfurther comprising a second response element.

In some embodiments, the second response element can comprise an HShresponse element. For example, a HSh response element comprising orconsisting of the nucleotide sequence set forth as SEQ ID NO: 111, or asequence at least 90% (such as at least 91%, at least 92%, at least 93%,at least 94%, at least 95%, at least 98%, or at least 99%) identicalthereto.

In some embodiments, the second response element can comprise a 5′HSresponse element. For example, a 5′HS response element comprising orconsisting of the nucleotide sequence set forth as nucleotides 6-32 ofSEQ ID NO: 111, or a sequence at least 90% (such as at least 91%, atleast 92%, at least 93%, at least 94%, at least 95%, at least 98%, or atleast 99%) identical thereto.

In some embodiments, the second response element can comprise a 3′HSresponse element. For example, a 3′HS response element comprising orconsisting of the nucleotide sequence set forth as nucleotides 44-68 ofSEQ ID NO: 111, or a sequence at least 90% (such as at least 91%, atleast 92%, at least 93%, at least 94%, at least 95%, at least 98%, or atleast 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 102 (HSh-HCB), or a sequence at least 90% (such as atleast 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 104 (5′HSh-HCB), or a sequence at least 90% (such as atleast 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 103 (3′HSh-HCB),

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 7 (ABP-HP1-God-TSS), or a sequence at least 90% (such asat least 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 105 (HSh-SynO-TSS), or a sequence at least 90% (such as atleast 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 106 (sHS-SynO-TSS), or a sequence at least 90% (such as atleast 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 107 (Agro), or a sequence at least 90% (such as at least91%, at least 92%, at least 93%, at least 94%, at least 95%, at least98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 108 (HS-SynO-TSS), or a sequence at least 90% (such as atleast 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 112 (HNF1-ShortABPExact-SynO-TSS-Int), or a sequence atleast 90% (such as at least 91%, at least 92%, at least 93%, at least94%, at least 95%, at least 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 5 (shortABP-HP1-God-TSS), or a sequence at least 90% (suchas at least 91%, at least 92%, at least 93%, at least 94%, at least 95%,at least 98%, or at least 99%) identical thereto.

In some embodiments, the recombinant nucleic acid molecule comprises apromoter comprising or consisting of the nucleic acid sequence set forthas SEQ ID NO: 7 (ABP-HP1-God-TSS), or a sequence at least 90% (such asat least 91%, at least 92%, at least 93%, at least 94%, at least 95%, atleast 98%, or at least 99%) identical thereto.

The disclosed promoters can be utilized in any situation whereliver-specific transcription is desired. In several embodiments, any oneof the disclosed promoters can be included on a vector (such as an AAVvector) for gene therapy methods where liver-specific expression of atransgene is desired, such as liver specific expression of a clottingfactor as disclosed herein.

III. Recombinant Nucleic Acid Molecules Encoding Clotting Factors

The blood clotting system is a proteolytic cascade. Blood clottingfactors are present in the plasma as a zymogen, in other words in aninactive form, which on activation undergoes proteolytic cleavage torelease the active factor form the precursor molecule. The ultimate goalis to produce thrombin. Thrombin converts fibrinogen into fibrin, whichforms a clot.

Factor X is the first molecule of the common pathway and is activated bya complex of molecules containing activated fix, fVIII, calcium, andphospholipids which are on the platelet surface. FVIII is activated bythrombin, and it facilitates the activation of factor X by fiXa. FVIII,contains multiple domains (A1-A2-B-ap-A3-C1-C2) and circulates in bloodin an inactivated form bound to von Willebrand factor (VWF). The C2domain is involved with fVIII binding to VWF. Thrombin cleaves fVIIIcausing dissociation with VWF ultimately leading to fibrin formationthrough fIX. Congenital hemophilia A is associated with geneticmutations in the fVIII gene and results in impaired clotting due tolower than normal levels of circulating fVIII. Hemophilia B is similarlyassociated with genetic mutations in the fIX gene.

FVIII domain boundaries refer to the human fVIII amino acid sequencenumbering as follows; residues 1-19 (Signal Sequence), 20-391 (A1),392-759 (A2), 760-1667 (B), 1668-1708 (ap), 1709-2038 (A3), 2039-2191(C1) and 2192-2351 (C2) (see Gitschier et al., Nature, 1984, 312,326-330) of SEQ ID NO: 1:

MQIELSTCFFLCLLRFCFSATRRYYLGAVELSWDYMQSDLGELPVDARFPPRVPKSFPFNTSVVYKKTLFVEFTDHLFNIAKPRPPWMGLLGPTIQAEVYDTVVITLKNMASHPVSLHAVGVSYWKASEGAEYDDQTSQREKEDDKVFPGGSHTYVWQVLKENGPMASDPLCLTYSYLSHVDLVKDLNSGLIGALLVCREGSLAKEKTQTLHKFILLFAVFDEGKSWHSETKNSLMQDRDAASARAWPKMHTVNGYVNRSLPGLIGCHRKSVYWHVIGMGTTPEVHSIFLEGHTFLVRNHRQASLEISPITFLTAQTLLMDLGQFLLFCHISSHQHDGMEAYVKVDSCPEEPQLRMKNNEEAEDYDDDLTDSEMDVVRFDDDNSPSFIQIRSVAKKHPKTWVHYIAAEEEDWDYAPLVLAPDDRSYKSQYLNNGPQRIGRKYKKVRFMAYTDETFKTREAIQHESGILGPLLYGEVGDTLLIIFKNQASRPYNIYPHGITDVRPLYSRRLPKGVKHLKDFPILPGEIFKYKWTVTVEDGPTKSDPRCLTRYYSSFVNMERDLASGLIGPLLICYKESVDQRGNQIMSDKRNVILFSVFDENRSWYLTENIQRFLPNPAGVQLEDPEFQASNIMHSINGYVFDSLQLSVCLHEVAYWYILSIGAQTDFLSVFFSGYTFKHKMVYEDTLTLFPFSGETVFMSMENPGLWILGCHNSDFRNRGMTALLKVSSCDKNTGDYYEDSYEDISAYLLSKNNAIEPRSFSQNSRHPSTRQKQFNATTIPENDIEKTDPWFAHRTPMPKIQNVSSSDLLMLLRQSPTPHGLSLSDLQEAKYETFSDDPSPGAIDSNNSLSEMTHFRPQLHHSGDMVFTPESGLQLRLNEKLGTTAATELKKLDFKVSSTSNNLISTIPSDNLAAGTDNTSSLGPPSMPVHYDSQLDTTLFGKKSSPLTESGGPLSLSEENNDSKLLESGLMNSQESSWGKNVSSTESGRLFKGKRAHGPALLTKDNALFKVSISLLKTNKTSNNSATNRKTHIDGPSLLIENSPSVWQNILESDTEFKKVTPLIHDRMLMDKNATALRLNHMSNKTTSSKNMEMVQQKKEGPIPPDAQNPDMSFFKMLFLPESARWIQRTHGKNSLNSGQGPSPKQLVSLGPEKSVEGQNFLSEKNKVVVGKGEFTKDVGLKEMVFPSSRNLFLTNLDNLHENNTHNQEKKIQEEIEKKETLIQENVVLPQIHTVTGTKNFMKNLFLLSTRQNVEGSYDGAYAPVLQDFRSLNDSTNRTKKHTAHFSKKGEEENLEGLGNQTKQIVEKYACTTRISPNTSQQNFVTQRSKRALKQFRLPLEETELEKRIIVDDTSTQWSKNMKHLTPSTLTQIDYNEKEKGAITQSPLSDCLTRSHSIPQANRSPLPIAKVSSFPSIRPIYLTRVLFQDNSSHLPAASYRKKDSGVQESSHFLQGAKKNNLSLAILTLEMTGDQREVGSLGTSATNSVTYKKVENTVLPKPDLPKTSGKVELLPKVHIYQKDLFPTETSNGSPGHLDLVEGSLLQGTEGAIKWNEANRPGKVPFLRVATESSAKTPSKLLDPLAWDNHYGTQIPKEEWKSQEKSPEKTAFKKKDTILSLNACESNHAIAAINEGQNKPEIEVTWAKQGRTERLCSQNPPVLKRHQREITRTTLQSDQEEIDYDDTISVEMKKEDFDIYDEDENQSPRSFQKKTRHYFIAAVERLWDYGMSSSPHVLRNRAQSGSVPQFKKVVFQEFTDGSFTQPLYRGELNEHLGLLGPYIRAEVEDNIMVTFRNQASRPYSFYSSLISYEEDQRQGAEPRKNFVKPNETKTYFWKVQHHMAPTKDEFDCKAWAYFSDVDLEKDVHSGLIGPLLVCHTNTLNPAHGRQVTVQEFALFFTIFDETKSWYFTENMERNCRAPCNIQMEDPTFKENYRFHAINGYIMDTLPGLVMAQDQRIRWYLLSMGSNENIHSIHFSGHVFTVRKKEEYKMALYNLYPGVFETVEMLPSKAGIWRVECLIGEHLHAGMSTLFLVYSNKCQTPLGMASGHIRDFQITASGQYGQWAPKLARLHYSGSINAWSTKEPFSWIKVDLLAPMIIHGIKTQGARQKFSSLYISQFIIMYSLDGKKWQTYRGNSTGTLMVFFGNVDSSGIKHNIFNPPIIARYIRLHPTHYSIRSTLRMELMGCDLNSCSMPLGMESKAISDAQITASSYFTNMFATWSPSKARLHLQGRSNAWRPQVNNPKEWLQVDFQKTMKVTGVTTQGVKSLLTSMYVKEFLISSSQDGHQWTLFFQNGKVKVFQGNQDSFTPVVNSLDPPLLTRYLRIHPQSWVHQIALRMEVLGCEAQDL Y

As discussed in Example 1, the cDNA nucleotide sequences coding forfVIII variants ET3 and HSQ were improved by implementing a codon usagebias specific for the human liver cell as compared to naturallyoccurring nucleotide sequence coding for the corresponding non-codonoptimized sequence for a human. Additional changes were also made toimprove translation efficacy, such as optimization of GC content, mRNAsecondary structure, premature PolyA sites, RNA instability motif,stable free energy of mRNA, internal chi sites, ribosomal binding sites,cryptic splicing sites, negative CpG islands, SD sequence, TATA boxes,and cyptic terminal signals.

In addition, CpG DNA motifs were removed because they may lead to genemethylation and silencing. See Bird, DNA methylation and the frequencyof CpG in animal DNA, 1980, Nucleic Acids Res, 8: 1499-1504. Codons weresubstituted with the most highly used human/liver alternative that didnot result in the formation of a 5′-CG-3′ dinucleotide in the sequence.CpG removal can also reduce any immune response to a vector includingthe modified transgene, enhancing the safety and efficacy of the vector.See J Clin Invest. 2013, 123(7):2994-3001, entitled “CpG-depletedadeno-associated virus vectors evade immune detection.”

ET3 is a B domain deleted (BDD) fVIII hybrid that contains human andporcine domains, i.e., sequence (A1 and A3 porcine, see FIGS. 1A and 1B)with a linker in the deleted B domain ET3 utilizes a 24 amino acidporcine sequence-derived OL linker sequence, i.e., porcine-derivedsequence SFAQNSRPPSASAPKPPVLRRHQR (SEQ ID NO: 23). HSQ is a human fVIIIvariant wherein the BDD human fVIII protein is substituted with a 14amino acid human-derived SQ linker SFSQNPPVLKRHQR (SEQ ID NO: 22). HSQamino acid sequence is provided as SEQ ID NO: 3. Both HSQ and ET3contain the RHQR (SEQ ID NO: 24) recognition sequence for PACE/furinprocessing sequence for the B-domain.

As discussed in Example 1, the nucleotide sequence encoding ET3 wascodon-optimized for expression in human liver. An exemplary liver codonoptimized ET3 sequence is provided as SEQ ID NO: 12. In someembodiments, a recombinant nucleic acid molecule is provided comprisingthe nucleotide sequence set forth as SEQ ID NO: 12, or a sequence atleast 90% (such as at least 95%) identical thereto. Further, CpG motifswithin the codon-optimized ET3 sequence were removed, to provide the CpGdeleted, liver codon optimized ET3 sequence set forth as SEQ ID NO: 11.In some embodiments, a recombinant nucleic acid molecule is providedcomprising the nucleotide sequence set forth as SEQ ID NO: 11, or asequence at least 90% (such as at least 95%) identical thereto.

As discussed in Example 1, the nucleotide sequence encoding HSQ wascodon-optimized for expression in human liver. Further, CpG motifswithin the codon-optimized HSQ sequence were removed, to provide the CpGdeleted, liver codon optimized HSQ sequence set forth as SEQ ID NO: 2.In some embodiments, a recombinant nucleic acid molecule is providedcomprising the nucleotide sequence set forth as SEQ ID NO: 2, or asequence at least 90% (such as at least 95%) identical thereto.

Additionally, the nucleotide sequences encoding ET3 and HSQ wereoptimized for expression in myeloid cells. An exemplary CpG deleted,myeloid codon-optimized ET3 sequence is provided as SEQ ID NO: 125. Insome embodiments, a recombinant nucleic acid molecule is providedcomprising the nucleotide sequence set forth as SEQ ID NO: 125, or asequence at least 90% (such as at least 95%) identical thereto. Anexemplary CpG deleted, myeloid codon-optimized HSQ sequence is providedas SEQ ID NO: 126. In some embodiments, a recombinant nucleic acidmolecule is provided comprising the nucleotide sequence set forth as SEQID NO: 126, or a sequence at least 90% (such as at least 95%) identicalthereto.

In additional embodiments, fIX coding sequence variants are providedthat are designed for high levels of expression when the transgene isexpressed from the liver, which is the target tissue of manyflX-targeted gene therapy strategies. To create this coding sequence,one utilizes a liver-directed codon optimization strategy.

As discussed in Example 1, the nucleotide sequence coding for flX wasoptimized by implementing a codon usage bias specific for the humanliver cell as compared to naturally occurring nucleotide sequence codingfor the corresponding non-codon optimized sequence for a human.

Additional changes were also made to improve Translation efficacy, suchas optimization of GC content, mRNA secondary structure, premature PolyAsites, RNA instability motif, stable free energy of mRNA, internal chisites, ribosomal binding sites, cryptic splicing sites, negative CpGislands, SD sequence, TATA boxes, and cyptic terminal signals.

In addition to adjusting the codon usage bias, the resulting sequencesare further modified to remove CpG motifs which may inhibit efficientexpression of the transgene. Further, in some embodiments, therecombinant flX nucleic acid molecule can encode flX with the K5Amutation (Darrel Stafford collagen binding mutation, Gui et al. Blood.2002, 100(1):153-8). In certain embodiments, the recombinant flX nucleicacid molecule can encode flX with the R338L mutation (Padua mutation),which is a naturally occurring gain of function mutation that has beenshown to improve the specific activity of flX by 8-fold. Sequencevariants were additionally created to reflect two major polymorphisms offlX at residue 148, including alanine or threonine. In some embodiments,these flX sequences may be grafted into liver-directed AAV as eithersingle-stranded or self-complimentary double stranded transgene designs.

Exemplary recombinant nucleic acid sequences encoding fVIII or flXproteins, or variants thereof, that are modified for tissue-specificexpression are discussed in Example 1.

SEQ ID NO: 12 provides an exemplary liver codon optimized ET3 sequence.In some embodiments, a recombinant nucleic acid molecule is providedthat comprises or consists of the nucleic acid sequence set forth as SEQID NO: 12, or a sequence at least 90% (such as at least 95%) identicalthereto.

SEQ ID NO: 11 provides an exemplary CpG deleted, liver codon optimizedET3 sequence. In some embodiments, a recombinant nucleic acid moleculeis provided that comprises or consists of the nucleic acid sequence setforth as SEQ ID NO: 11, or a sequence at least 90% (such as at least95%) identical thereto.

SEQ ID NO: 2 provides an exemplary CpG deleted, liver codon optimizedHSQ sequence. In some embodiments, a recombinant nucleic acid moleculeis provided that comprises or consists of the nucleic acid sequence setforth as SEQ ID NO: 2, or a sequence at least 90% (such as at least 95%)identical thereto.

SEQ ID NO: 125 provides an exemplary CpG deleted, myeloid codonoptimized ET3 sequence. In some embodiments, a recombinant nucleic acidmolecule is provided that comprises or consists of the nucleic acidsequence set forth as SEQ ID NO: 125, or a sequence at least 90% (suchas at least 95%) identical thereto.

SEQ ID NO: 126 provides an exemplary CpG deleted, myeloid codonoptimized HSQ sequence. In some embodiments, a recombinant nucleic acidmolecule is provided that comprises or consists of the nucleic acidsequence set forth as SEQ ID NO: 125, or a sequence at least 90% (suchas at least 95%) identical thereto.

Exemplary recombinant nucleic acid sequences encoding fIX proteins, orvariants thereof, that are modified for tissue-specific expression arediscussed in Example 1.

SEQ ID NO: 124 provides an exemplary liver codon optimized fIX sequencewith Padua/Malmo mutations and no CpG. In some embodiments, arecombinant nucleic acid molecule is provided that comprises or consistsof the nucleic acid sequence set forth as SEQ ID NO: 124, or a sequenceat least 90% (such as at least 95%) identical thereto.

SEQ ID NO: 8 provides an exemplary liver-codon optimized fiX sequencewith no CpG and encoding A582 modifications. In some embodiments, arecombinant nucleic acid molecule is provided that comprises or consistsof the nucleic acid sequence set forth as SEQ ID NO: 8, or a sequence atleast 90% (such as at least 95%) identical thereto.

SEQ ID NO: 9 provides an exemplary liver codon optimized fiX sequencewith no CpG and including Padua and A582 modifications. In someembodiments, a recombinant nucleic acid molecule is provided thatcomprises or consists of the nucleic acid sequence set forth as SEQ IDNO: 9, or a sequence at least 90% (such as at least 95%) identicalthereto.

SEQ ID NO: 10 provides an exemplary liver codon optimized fiX sequencewith Padua/Malmo mutations and no CpG. In some embodiments, arecombinant nucleic acid molecule is provided that comprises or consistsof the nucleic acid sequence set forth as SEQ ID NO:10, or a sequence atleast 90% (such as at least 95%) identical thereto.

SEQ ID NO: 127 provides an exemplary human codon optimized fIX sequencewith Padua/Malmo mutations and no CpG. In some embodiments, arecombinant nucleic acid molecule is provided that comprises or consistsof the nucleic acid sequence set forth as SEQ ID NO:127, or a sequenceat least 90% (such as at least 95%) identical thereto.

Any of the above discussed recombinant nucleic acid molecules encoding afVIII or fIX protein, or variant thereof, can be included in an vector(such as a AAV vector) as described herein for embodiments whereexpression of a fVIII or FIX protein or variant thereof is of interest.

In some embodiments, an isolated protein is provided comprising an aminoacid sequence encoded by one of SEQ ID NOs: 8, 9, or 10, such as theamino acid sequences set forth as SEQ ID NOs: 17-18 below. In someembodiments, an isolated protein is provided comprising an amino acidsequence set forth as SEQ ID NO: 17, or an amino acid sequence at least90% (such as at least 95%) identical thereto having fiX activity. Insome embodiments, an isolated protein is provided comprising an aminoacid sequence set forth as SEQ ID NO: 18, or an amino acid sequence atleast 90% (such as at least 95%) identical thereto having fIX activity.In some embodiments, an isolated protein is provided comprising an aminoacid sequence set forth as SEQ ID NO: 19, or an amino acid sequence atleast 90% (such as at least 95%) identical thereto having fiX activity.

SEQ ID NO: 8 encodes the amino acid sequence set forth as SEQ ID NO: 17:MQRVNMIMAESPGLITICLLGYLLSAECTVFLDHENANKILNRPKRYNSGKLEEFVQGNLERECMEEKCSFEEAREVFENTERTTEFWKQYVDGDQCESNPCLNGGSCKDDINSYECWCPFGFEGKNCELDVTCNIKNGRCEQFCKNSADNKVVCSCTEGYRLAENQKSCEPAVPFPCGRVSVSQTSKLTRAEAVFPDVDYVNSTEAETILDNITQSTQSFNDFTRVVGGEDAKPGQFPWQVVLNGKVDAFCGGSIVNEKWIVTAAHCVETGVKITVVAGEHNIEETEHTEQKRNVIRIIPHHNYNAAINKYNHDIALLELDEPLVLNSYVTPICIADKEYTNIFLKFGSGYVSGWGRVFHKGRSALVLQYLRVPLVDRATCLRSTKFTIYNNMFCAGFHEGGRDSCQGDSGGPHVTEVEGTSFLTGIISWGEECAMKGKYGIYTKVSRY VNWIKEKTKLTSEQ ID NO: 9 encodes the amino acid sequence set forth as SEQ ID NO: 18:MQRVNMIMAESPGLITICLLGYLLSAECTVFLDHENANKILNRPKRYNSGKLEEFVQGNLERECMEEKCSFEEAREVFENTERTTEFWKQYVDGDQCESNPCLNGGSCKDDINSYECWCPFGFEGKNCELDVTCNIKNGRCEQFCKNSADNKVVCSCTEGYRLAENQKSCEPAVPFPCGRVSVSQTSKLTRAEAVFPDVDYVNSTEAETILDNITQSTQSFNDFTRVVGGEDAKPGQFPWQVVLNGKVDAFCGGSIVNEKWIVTAAHCVETGVKITVVAGEHNIEETEHTEQKRNVIRIIPHHNYNAAINKYNHDIALLELDEPLVLNSYVTPICIADKEYTNIFLKFGSGYVSGWGRVFHKGRSALVLQYLRVPLVDRATCLLSTKFTIYNNMFCAGFHEGGRDSCQGDSGGPHVTEVEGTSFLTGIISWGEECAMKGKYGIYTKVSRY VNWIKEKTKLTSEQ ID NO: 10 encodes the amino acid sequenceset forth as SEQ ID NO: 19:MQRVNMIMAESPGLITICLLGYLLSAECTVFLDHENANKILNRPKRYNSGKLEEFVQGNLERECMEEKCSFEEAREVFENTERTTEFWKQYVDGDQCESNPCLNGGSCKDDINSYECWCPFGFEGKNCELDVTCNIKNGRCEQFCKNSADNKVVCSCTEGYRLAENQKSCEPAVPFPCGRVSVSQTSKLTRAETVFPDVDYVNSTEAETILDNITQSTQSFNDFTRVVGGEDAKPGQFPWQVVLNGKVDAFCGGSIVNEKWIVTAAHCVETGVKITVVAGEHNIEETEHTEQKRNVIRIIPHHNYNAAINKYNHDIALLELDEPLVLNSYVTPICIADKEYTNIFLKFGSGYVSGWGRVFHKGRSALVLQYLRVPLVDRATCLLSTKFTIYNNMFCAGFHEGGRDSCQGDSGGPHVTEVEGTSFLTGIISWGEECAMKGKYGIYTKVSRY VNWIKEKTKLT

Exemplary nucleic acids can be prepared by cloning techniques, or can begenerated synthetically. Examples of appropriate cloning and sequencingtechniques, and instructions sufficient to direct persons of skillthrough many cloning exercises are known (see, e.g., Sambrook et al.(Molecular Cloning: A Laboratory Manual, 4^(th) ed, Cold Spring Harbor,N.Y., 2012) and Ausubel et al. (In Current Protocols in MolecularBiology, John Wiley & Sons, New York, through supplement 104, 2013).Product information from manufacturers of biological reagents andexperimental equipment also provide useful information. Suchmanufacturers include the SIGMA Chemical Company (Saint Louis, Mo.), R&DSystems (Minneapolis, Minn.), Pharmacia Amersham (Piscataway, N.J.),CLONTECH Laboratories, Inc. (Palo Alto, Calif.), Chem Genes Corp.,Aldrich Chemical Company (Milwaukee, Wis.), Glen Research, Inc., GIBCOBRL Life Technologies, Inc. (Gaithersburg, Md.), FlukaChemica-Biochemika Analytika (Fluka Chemie AG, Buchs, Switzerland),Invitrogen (Carlsbad, Calif.), and Applied Biosystems (Foster City,Calif.), as well as many other commercial sources known to one of skill.

Nucleic acids can also be prepared by amplification methodsAmplification methods include polymerase chain reaction (PCR), theligase chain reaction (LCR), the transcription-based amplificationsystem (TAS), the self-sustained sequence replication system (3SR). Awide variety of cloning methods, host cells, and in vitro amplificationmethodologies are well known to persons of skill.

IV. Recombinant Vectors and Gene Therapy Applications

The nucleic acid and promotor sequences disclosed herein are useful inproduction of vectors (such as rAAV vectors), and are also useful asantisense delivery vectors, gene therapy vectors, or vaccine vectors. Incertain embodiments, the disclosure provides for gene delivery vectors,and host cells which contain the nucleic acid sequences disclosedherein. In some embodiments, the selected vector may be delivered to asubject by any suitable method, including intravenous injection, ex-vivotransduction, transfection, electroporation, liposome delivery, membranefusion techniques, high velocity DNA-coated pellets, viral infection, orprotoplast fusion, to introduce a transgene into the subject.

In certain embodiments, the disclosure relates to virus particle, e.g.,capsids, containing the nucleic acid sequences encoding promotors andproteins disclosed herein. The virus particles, capsids, and recombinantvectors are useful in delivery of a heterologous gene or other nucleicacid sequences to a target cell. The nucleic acids may be readilyutilized in a variety of vector systems, capsids, and host cells. Incertain embodiments, the nucleic acids are in vectors contained within acapsid comprising cap proteins, including AAV capsid proteins vp1, vp2,vp3 and hypervariable regions.

In certain embodiments, the nucleic acids disclosed herein may be a partof any genetic element (vector) which may be delivered to a host cell,e.g., naked DNA, a plasmid, phage, transposon, cosmid, episome, aprotein in a non-viral delivery vehicle (e.g., a lipid-based carrier),virus, etc. which transfer the sequences carried thereon.

In certain embodiments, a vector may be a lentivirus based (containinglentiviral genes or sequences) vector, e.g., having nucleic acidsequences derived from VSVG or GP64 pseudotypes or both. In certainembodiments, the nucleic acid sequences derived from VSVG or GP64pseudotypes may be at least one or two or more genes or gene fragmentsof more than 1000, 500, 400, 300, 200, 100, 50, or 25 continuousnucleotides or nucleotides sequences with greater than 50, 60, 70, 80,90, 95 or 99% identity to the gene or fragment.

In some embodiments, a method of inducing blood clotting in a subject inneed thereof is provided. The method comprises administering to thesubject a therapeutically effective amount of a vector (such as an AAVvector) encoding a clotting factor as described herein. In someembodiments, the subject is a subject with a clotting disorder, such ashemophilia A or hemophilia B. In some embodiments, the clotting disorderis hemophilia A and the subject is administered a vector comprising anucleic acid molecule encoding a protein with fVIII activity. In otherembodiments, the clotting disorder is hemophilia B and the subject isadministered a vector comprising a nucleic acid molecule encoding aprotein with fIX activity.

In some embodiments, the nucleic acid and promotor sequences disclosedherein are useful in production of AAV vectors. AAV belongs to thefamily Parvoviridae and the genus Dependovirus. AAV is a small,non-enveloped virus that packages a linear, single-stranded DNA genome.Both sense and antisense strands of AAV DNA are packaged into AAVcapsids with equal frequency.

The AAV genome is characterized by two inverted terminal repeats (ITRs)that flank two open reading frames (ORFs). In the AAV2 genome, forexample, the first 125 nucleotides of the ITR are a palindrome, whichfolds upon itself to maximize base pairing and forms a T-shaped hairpinstructure. The other 20 bases of the ITR, called the D sequence, remainunpaired. The ITRs are cis-acting sequences important for AAV DNAreplication; the ITR is the origin of replication and serves as a primerfor second-strand synthesis by DNA polymerase. The double-stranded DNAformed during this synthesis, which is called replicating-form monomer,is used for a second round of self-priming replication and forms areplicating-form dimer. These double-stranded intermediates areprocessed via a strand displacement mechanism, resulting insingle-stranded DNA used for packaging and double-stranded DNA used fortranscription. Located within the ITR are the Rep binding elements and aterminal resolution site (TRS). These features are used by the viralregulatory protein Rep during AAV replication to process thedouble-stranded intermediates. In addition to their role in AAVreplication, the ITR is also essential for AAV genome packaging,transcription, negative regulation under non-permissive conditions, andsite-specific integration (Daya and Berns, Clin Microbiol Rev21(4):583-593, 2008).

The left ORF of AAV contains the Rep gene, which encodes fourproteins—Rep78, Rep 68, Rep52 and Rep40. The right ORF contains the Capgene, which produces three viral capsid proteins (VP1, VP2 and VP3). TheAAV capsid contains 60 viral capsid proteins arranged into anicosahedral symmetry. VP1, VP2 and VP3 are present in a 1:1:10 molarratio (Daya and Berns, Clin Microbiol Rev 21(4):583-593, 2008).

AAV vectors typically contain a transgene expression cassette betweenthe ITRs that replaces the rep and cap genes. Vector particles areproduced by the co-transfection of cells with a plasmid containing thevector genome and a packaging/helper construct that expresses the repand cap proteins in trans. During infection, AAV vector genomes enterthe cell nucleus and can persist in multiple molecular states. Onecommon outcome is the conversion of the AAV genome to a double-strandedcircular episome by second-strand synthesis or complementary strandpairing.

In the context of AAV vectors, the disclosed vectors typically have arecombinant genome comprising the following structure:

(5′AAV ITR)-(promoter)-(transgene)-(3′AAV ITR)

As discussed above, these recombinant AAV vectors contain a transgeneexpression cassette between the ITRs that replaces the rep and capgenes. Vector particles are produced, for example, by theco-transfection of cells with a plasmid containing the recombinantvector genome and a packaging/helper construct that expresses the repand cap proteins in trans. For example, in some embodiments, therecombinant AAV vector can have a genome with a structure set forth asone of:

(5′AAV ITR) - (HCB) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (fix, Seq_10) - (3′AAV ITR) (5′AAV ITR) - (sHS-SynO-TSS) - (transgene) - (3′AAV ITR) (5′AAV ITR) - (sHS-SynO-TSS) - (fVIII) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fVIII-B-domain deleted) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (ET3) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (ET3, Seq_12) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (ET3, Seq_11) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (HSQ) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (HSQ, Seq_2) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fiX) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fix, Seq_124) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fix, Seq_8) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fix, Seq_9) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (fix, Seq_10) - (3′AAV ITR) 

The transgene can be flanked by regulatory sequences such as a 5′ Kozaksequence and/or a 3′ polyadenylation signal. For example, in someembodiments, the recombinant AAV vector can have a genome with astructure set forth as one of:

(5′AAV ITR) - (HCB) - (Kozak) - (transgene) - (polyA signal) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fIX, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fIX, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fIX, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HCB) - (Kozak) - (fIX, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fix, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fix, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fix, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-HCB) - (Kozak) - (fIX, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fix, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fix, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fix, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (5′HSh-HCB) - (Kozak) - (fix, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fix, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fix, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fix, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (3′HSh-HCB) - (Kozak) - (fIX, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fIX, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fIX, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fIX, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (ABP-HP1-God-TSS) - (Kozak) - (fIX, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fix, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fix, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fix, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (HSh-SynO-TSS) - (Kozak) - (fIX, Seq_10) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS-SynO-TSS) - (Kozak) - (transgene) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS-SynO-TSS) - (Kozak) - (fVIII) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fVIII-B-domain deleted) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (ET3) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (ET3, Seq_12) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (ET3, Seq_11) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (HSQ) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (HSQ, Seq_2) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fIX) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fix, Seq_124) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fix, Seq_8) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fix, Seq_9) - (polyA signal) - (3′AAV ITR) (5′AAV ITR) - (sHS -SynO-TSS) - (Kozak) - (fix, Seq_10) - (polyA signal) - (3′AAV ITR) 

The AAV ITRs, and other selected AAV components described herein, may bereadily selected from among any AAV serotype, including, withoutlimitation, AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9 andfunction variants thereof. These ITRs or other AAV components may bereadily isolated using techniques available to those of skill in the artfrom an AAV serotype. Such AAV may be isolated or obtained fromacademic, commercial, or public sources (e.g., the American Type CultureCollection, Manassas, Va.). Alternatively, the AAV sequences may beobtained through synthetic or other suitable means by reference topublished sequences such as are available in the literature or indatabases such as, e.g., GenBank, PubMed, or the like.

In some embodiments, the vector can be a recombinant AAV vectorcomprising a genome comprising a nucleic acid molecule encoding any ofthe liver-specific promoters provided herein (such as the HCB promoter,SEQ ID NO: 4) operably linked to a heterologous nucleic moleculeencoding a fVIII variant, wherein the heterologous nucleic acid moleculecomprises or consists of the nucleic acid sequence set forth as SEQ IDNO: 2, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ ID NO: 126,or a nucleic acid sequence at least 90% identical to SEQ ID NO: 2, SEQID NO: 11, SEQ ID NO: 12, SEQ ID NO: 125, or SEQ ID NO: 126. Is severalsuch embodiments, the recombinant AAV genome (from 5′ to 3′ ITR) is nomore than 5.1, 5.0, 4.9, 4.8, 4.7, 4.6, or 4.5 kb in length.

In some embodiments, the vector can be a recombinant AAV vectorcomprising a genome comprising a nucleic acid molecule encoding any ofthe liver-specific promoters provided herein (such as the HCB promoter,SEQ ID NO: 4) operably linked to a heterologous nucleic moleculeencoding a fIX variant, wherein the heterologous nucleic acid moleculecomprises or consists of the nucleic acid sequence set forth as SEQ IDNO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 124, or SEQ ID NO: 127,or a nucleic acid sequence at least 90% identical SEQ ID NO: 8, SEQ IDNO: 9, SEQ ID NO: 10, SEQ ID NO: 124, or SEQ ID NO: 127. Is several suchembodiments, the recombinant AAV genome (from 5′ to 3′ ITR) is no morethan 5.1, 5.0, 4.9, 4.8, 4.7, 4.6, or 4.5 kb in length.

AAV is currently one of the most frequently used viruses for genetherapy. Although AAV infects humans and some other primate species, itis not known to cause disease and elicits a very mild immune response.Gene therapy vectors that utilize AAV can infect both dividing andquiescent cells and persist in an extrachromosomal state withoutintegrating into the genome of the host cell. Because of theadvantageous features of AAV, the present disclosure contemplates theuse of AAV for the recombinant nucleic acid molecules and methodsdisclosed herein.

AAV possesses several desirable features for a gene therapy vector,including the ability to bind and enter target cells, enter the nucleus,the ability to be expressed in the nucleus for a prolonged period oftime, and low toxicity. However, the small size of the AAV genome limitsthe size of heterologous DNA that can be incorporated. To minimize thisproblem, AAV vectors have been constructed that do not encode Rep andthe integration efficiency element (IEE). The ITRs are retained as theyare cis signals required for packaging (Daya and Berns, Clin MicrobiolRev 21(4):583-593, 2008).

Methods for producing rAAV suitable for gene therapy are known (see, forexample, U.S. Patent Application Nos. 2012/0100606; 2012/0135515;2011/0229971; and 2013/0072548; and Ghosh et al., Gene Ther13(4):321-329, 2006), and can be utilized with the recombinant nucleicacid molecules and methods disclosed herein.

In some embodiments, the nucleic acids disclosed herein are part of anexpression cassette or transgene. See e.g., US Pat. App. Pub.20150139953. The expression cassette is composed of a transgene andregulatory sequences, e.g., promotor and 5′ and 3′ AAV inverted terminalrepeats (ITRs). In one desirable embodiment, the ITRs of AAV serotype 2or 8 are used. However, ITRs from other suitable serotypes may beselected. An expression cassette is typically packaged into a capsidprotein and delivered to a selected host cell.

In some embodiments, the disclosure provides for a method of generatinga recombinant adeno-associated virus (AAV) having an AAV serotypecapsid, or a portion thereof. Such a method involves culturing a hostcell which contains a nucleic acid sequence encoding an adeno-associatedvirus (AAV) serotype capsid protein; a functional rep gene; anexpression cassette composed of AAV inverted terminal repeats (ITRs) anda transgene; and sufficient helper functions to permit packaging of theexpression cassette into the AAV capsid protein. See e.g., US Pat. App.Pub. 20150139953.

The components for culturing in the host cell to package an AAVexpression cassette in an AAV capsid may be provided to the host cell intrans. Alternatively, any one or more of the components (e.g.,expression cassette, rep sequences, cap sequences, and/or helperfunctions) may be provided by a stable host cell which has beenengineered to contain one or more of the required components usingmethods known to those of skill in the art. Most suitably, such a stablehost cell will contain the component(s) under the control of aninducible promoter. However, the required component(s) may be under thecontrol of a constitutive promoter. In still another alternative, aselected stable host cell may contain selected component(s) under thecontrol of a constitutive promoter and other selected component(s) underthe control of one or more inducible promoters. For example, a stablehost cell may be generated which is derived from 293 cells (whichcontain E1 helper functions under the control of a constitutivepromoter), but which contains the rep and/or cap proteins under thecontrol of inducible promoters. Still other stable host cells may begenerated by one of skill in the art.

In some embodiments, the disclosure relates to recombinant vectorscomprising a liver specific promotor nucleic acid sequence in operablecombination with transgene. The transgene is a nucleic acid sequence,heterologous to the vector sequences flanking the transgene, whichencodes a protein, or other product, of interest. The nucleic acidcoding sequence is operatively linked to regulatory components in amanner which permits transgene transcription, translation, and/orexpression in a host cell.

A typical transgene is a sequence encoding a product which is useful inbiology and medicine, such as proteins, peptides, RNA, enzymes, dominantnegative mutants, or catalytic RNAs. Desirable RNA molecules includemRNA, tRNA, dsRNA, ribosomal RNA, catalytic RNAs, siRNA, microRNA, smallhairpin RNA, trans-splicing RNA, and antisense RNAs. One example of auseful RNA sequence is a sequence which inhibits or extinguishesexpression of a targeted nucleic acid sequence in the treated animalTypically, suitable target sequences in include oncologic targets andviral diseases.

The transgene may be used to correct or ameliorate gene deficiencies,which may include deficiencies in which normal genes are expressed atless than normal levels or deficiencies in which the functional geneproduct is not expressed. A preferred type of transgene sequence encodesa therapeutic protein or polypeptide which is expressed in a host cell.The disclosure further contemplates using multiple transgenes, e.g., tocorrect or ameliorate a gene defect caused by a multi-subunit protein.In certain situations, a different transgene may be used to encode eachsubunit of a protein, or to encode different peptides or proteins. Thisis desirable when the size of the DNA encoding the protein subunit islarge, e.g., for an immunoglobulin, the platelet-derived growth factor,or a dystrophin protein. In order for the cell to produce themulti-subunit protein, a cell is infected with the recombinant viruscontaining each of the different subunits. Alternatively, differentsubunits of a protein may be encoded by the same transgene. In thiscase, a single transgene includes the DNA encoding each of the subunits,with the DNA for each subunit separated by an internal ribozyme entrysite (IRES). This is desirable when the size of the DNA encoding each ofthe subunits and cis-regulatory control regions such as a promoter,intron, polyA signal is small, e.g., the total size of the DNA encodingthe subunits and the IRES and cis-regulatory control regions is lessthan five kilobases. As an alternative to an IRES, the DNA may beseparated by sequences encoding a 2A peptide, which self-cleaves in apost-translational event. See, e.g., M. L. Donnelly, et al., J. Gen.Virol., 78(Pt 1):13-21 (January 1997); Furler, S., et al, Gene Ther.,8(11):864-873 (June 2001); Klump H., et al., Gene Ther., 8(10):811-817(May 2001). In certain embodiments, rAAV carrying the desiredtransgene(s) or subunits are co-administered to allow them toconcatamerize in vivo to form a single vector genome. In such anembodiment, a first AAV may carry an expression cassette which expressesa single transgene and a second AAV may carry an expression cassettewhich expresses a different transgene for co-expression in the hostcell. However, the selected transgene may encode any biologically activeproduct or other product, e.g., a product desirable for study.

The expression cassette can be carried on any suitable vector, e.g., aplasmid, which is delivered to a host cell. The plasmids useful in thisdisclosure may be engineered such that they are suitable for replicationand, optionally, integration in prokaryotic cells, mammalian cells, orboth. These plasmids (or other vectors carrying the 5′ AAVITR-heterologous molecule-3′ ITR) contain sequences permittingreplication of the expression cassette in eukaryotes and/or prokaryotesand selection markers for these systems. Preferably, the moleculecarrying the expression cassette is transfected into the cell, where itmay exist transiently. Alternatively, the expression cassette (carryingthe 5′ AAV ITR-heterologous molecule-3′ ITR) may be stably integratedinto the genome of the host cell, either chromosomally or as an episome.In certain embodiments, the expression cassette may be present inmultiple copies, optionally in head-to-head, head-to-tail, ortail-to-tail concatamers. Suitable transfection techniques are known andmay readily be utilized to deliver the expression cassette to the hostcell.

Generally, when delivering the vector comprising the expression cassetteby transfection, the vector and the relative amounts of vector DNA tohost cells may be adjusted, taking into consideration such factors asthe selected vector, the delivery method and the host cells selected. Inaddition to the expression cassette, the host cell contains thesequences which drive expression of the AAV capsid protein in the hostcell and rep sequences of the same serotype as the serotype of the AAVITRs found in the expression cassette, or a cross-complementingserotype. Although the molecule(s) providing rep and cap may exist inthe host cell transiently (i.e., through transfection), it is preferredthat one or both of the rep and cap proteins and the promoter(s)controlling their expression be stably expressed in the host cell, e.g.,as an episome or by integration into the chromosome of the host cell.

The packaging host cell also typically contains helper functions inorder to package the rAAV of the disclosure. Optionally, these functionsmay be supplied by a herpesvirus. Most desirably, the necessary helperfunctions are each provided from a human or non-human primate adenovirussource, such as those described above and/or are available from avariety of sources, including the American Type Culture Collection(ATCC), Manassas, Va. (US). The desired helper functions, can beprovided using any means that allows their expression in a cell.

Introduction into the host cell of the vector may be achieved by anymeans known in the art or as disclosed above, including transfection,infection, electroporation, liposome delivery, membrane fusiontechniques, high velocity DNA-coated pellets, viral infection andprotoplast fusion, among others. One or more of the adenoviral genes maybe stably integrated into the genome of the host cell, stably expressedas episomes, or expressed transiently. The gene products may all beexpressed transiently, on an episome or stably integrated, or some ofthe gene products may be expressed stably while others are expressedtransiently. Furthermore, the promoters for each of the adenoviral genesmay be selected independently from a constitutive promoter, an induciblepromoter or a native adenoviral promoter. The promoters may be regulatedby a specific physiological state of the organism or cell (i.e., by thedifferentiation state or in replicating or quiescent cells) or byexogenously added factors, for example.

Introduction of the molecules (as plasmids or viruses) into the hostcell may be accomplished using techniques known to the skilled artisan.In preferred embodiment, standard transfection techniques are used,e.g., CaPO₄ transfection or electroporation, and/or infection by hybridadenovirus/AAV vectors into cell lines such as the human embryonickidney cell line HEK 293 (a human kidney cell line containing functionaladenovirus E1 genes which provides trans-acting E1 proteins).

One of skill in the art will readily understand that the AAV techniquescan be adapted for use in these and other viral vector systems for invitro, ex vivo or in vivo gene delivery. The in certain embodiments thedisclosure contemplates the use of nucleic acids and vectors disclosedherein in a variety of rAAV and non-rAAV vector systems. Such vectorssystems may include, e.g., lentiviruses, retroviruses, poxviruses,vaccinia viruses, and adenoviral systems, among others.

In some embodiments, it is contemplated that viral particles, nucleicacids and vectors disclosed herein are useful for a variety of purposes,including for delivery of therapeutic molecules for gene expression oftherapeutic proteins.

Therapeutic proteins encoded by the nucleic acids (e.g., operably incombination with promoters) reported herein include those used fortreatment of hemophilia, including hemophilia B (including fIX) andhemophilia A (including fVIII and its variants, such as the light chainand heavy chain of the heterodimer and the B-deleted domain; U.S. Pat.Nos. 6,200,560 and 6,221,349). The Factor VIII gene codes for 2351 aminoacids and the protein has six domains, designated from the amino to theterminal carboxy terminus as A 1-A2-B-A3-C1-C2 [Wood et al, Nature,312:330 (1984); Vehar et al., Nature 312:337 (1984); and Toole et al,Nature, 342:337 (1984)]. Human fVIII is processed within the cell toyield a heterodimer primarily comprising a heavy chain containing theA1, A2 and B domains and a light chain containing the A3, C1 and C2domains. Both the single chain polypeptide and the heterodimer circulatein the plasma as inactive precursors, until activated by thrombincleavage between the A2 and B domains, which releases the B domain andresults in a heavy chain consisting of the A1 and A2 domains. The Bdomain is deleted in the activated procoagulant form of the protein.Additionally, in the native protein, two polypeptide chains (“a” and“b”), flanking the B domain, are bound to a divalent calcium cation.

A treatment option for a patient diagnosed with hemophilia A is theexogenous administration of recombinant fVIII sometimes referred to asfVIII replacement therapy. In some patients, this therapy can lead tothe development of antibodies that bind to the administered fVIIIprotein. Subsequently, the fVIII-antibody bound conjugates, typicallyreferred to as inhibitors, interfere with or retard the ability of fVIIIto cause blood clotting. Inhibitory autoantibodies also sometimes occurspontaneously in a subject that is not genetically at risk of havinghemophilia, termed acquired hemophilia. Inhibitory antibodies assays aretypically performed prior to exogenous fVIII treatment in order todetermine whether the anti-coagulant therapy will be effective.

A “Bethesda assay” has historically been used to quantitate theinhibitory strength the concentration of fVIII binding antibodies. Inthe assay, serial dilutions of plasma from a patient, e.g., prior tohaving surgery, are prepared and each dilution is mixed with an equalvolume of normal plasma as a source of fVIII. After incubating for acouple hours, the activities of fVIII in each of the diluted mixturesare measured. Having antibody inhibitor concentrations that preventfVIII clotting activity after multiple repeated dilutions indicates aheightened risk of uncontrolled bleeding. Patients with inhibitor titersafter about ten dilutions are felt to be unlikely to respond toexogenous fVIII infusions to stop bleeding. A Bethesda titer is definedas the reciprocal of the dilution that results in 50% inhibition ofFVIII activity present in normal human plasma. A Bethesda titer greaterthan 10 is considered the threshold of response to FVIII replacementtherapy.

In certain embodiments, the disclosure relates to methods of inducingblood clotting comprising administering an effective amount of a viralparticle or capsid comprising a vector comprising a nucleic acidencoding a blood clotting factor as disclosed herein to a subject inneed thereof.

In certain embodiments, the subject is diagnosed with hemophilia A or Bor acquired hemophilia or unlikely to respond to exogenous fVIIIinfusions.

In some embodiments, this disclosure relates to methods gene transferfor the treatment of hemophilia B using an adeno-associated viral (AAV)vector encoding human fiX as the gene delivery vehicle. While severalsuch AAV-based gene therapies for hemophilia B have entered into humanclinical trials, they have been hampered by low expression of thetherapeutic protein, clotting fix, after administration of the virusresulting on only partial correction of the disease. AAV vector toxicitylimits the dose of the virus that may be safely administered. Tosuccessfully transition to a clinically viable therapy, a vector shouldprovide efficacious expression of fIX at viral doses below the thresholdof toxicity.

Treating patients with inhibitors to fVIII has also been accomplished bymethods of immune tolerance induction (ITI) which typically involves thedaily infusion of fVIII until circulating inhibitor/antibody levelsdecline. However, 20-30% of patients fail to become tolerant after animmune tolerance induction (ITI) therapy. Persistence of fVIIIinhibitors is associated with increased risks of morbidity andmortality. In certain embodiments, the disclosure relates to methods ofimmune tolerance induction comprising administering an effective amountof a vector or a capsid as disclosed herein to a subject in needthereof.

In some embodiments, the therapeutic proteins encoded by the nucleicacids (e.g., operably in combination with promoters) reported hereincomprises first 57 base pairs of the fVIII heavy chain which encodes the10 amino acid signal sequence, as well as the human beta globinpolyadenylation sequence or growth hormone (hGH) polyadenylationsequence. In alternative embodiments, the A1 and A2 domains, as well as5 amino acids from the N-terminus of the B domain, and/or 85 amino acidsof the C-terminus of the B domain, as well as the A3, C1 and C2 domains.In yet other embodiments, the nucleic acids encoding fVIII heavy chainand light chain are provided in a single nucleic acid separated by 42nucleic acids coding for 14 amino acids of the B domain See U.S. Pat.No. 6,200,560.

As used herein, a therapeutically effective amount is an amount of AAVvector that produces sufficient amounts of fVIII to decrease the time ittakes for the blood of a subject to clot. Generally, severe hemophiliacshaving less than 1% of normal levels of fVIII have a whole bloodclotting time of greater than 60 minutes as compared to approximately 10minutes for non-hemophiliacs.

The present disclosure is not limited to any specific fVIII or fiX orother protein sequence reported herein. Many natural and recombinantforms of fVIII have been isolated and generated. Examples of naturallyoccurring and recombinant forms of fVII can be found in the patent andscientific literature including, U.S. Pat. Nos. 5,563,045, 5,451,521,5,422,260, 5,004,803, 4,757,006, 5,661,008, 5,789,203, 5,681,746,5,595,886, 5,045,455, 5,668,108, 5,633,150, 5,693,499, 5,587,310,5,171,844, 5,149,637, 5,112,950, 4,886,876, WO 94/11503, WO 87/07144, WO92/16557, WO 91/09122, WO 97/03195, WO 96/21035, WO 91/07490, EP 0 672138, EP 0 270 618, EP 0 182 448, EP 0 162 067, EP 0 786 474, EP 0 533862, EP 0 506 757, EP 0 874 057, EP 0 795 021, EP 0 670 332, EP 0 500734, EP 0 232 112, EP 0 160 457, Sanberg et al., Int. Congress of theWorld Fed. Of Hemophilia (1992), and Lind et al., Eur. J. Biochem.,232:19 (1995).

Furthermore, the disclosure is not limited to human fVIII. Indeed, it isintended that the present disclosure encompass fVIII from animals otherthan humans, including but not limited to companion animals (e.g.,canine, felines, and equines), livestock (e.g., bovines, caprines andovines), laboratory animals, marine mammals, large cats, etc.

The AAV vectors may contain a nucleic acid coding for fragments of fVIIIwhich is itself not biologically active, yet when administered into thesubject improves or restores the blood clotting time. For example, thefVIII protein comprises two polypeptide chains: a heavy chain and alight chain separated by a B-domain which is cleaved during processing.Co-transducing recipient cells with the FVIII heavy and light chainsleads to the expression of biologically active fVIII. Administration ofonly the chain defective is contemplated in patients because mosthemophiliacs contain a mutation or deletion in only one of the chains(e.g., heavy or light chain).

Thus, in certain embodiments, the disclosure relates to vectorsdisclosed herein having nucleic acids encoding a light chain containingthe A3, C1 and C2 domains or a heavy chain consisting of the A1 and A2domains.

Additional Description of Recombinant Vectors and Therapeutic Modalities

The recombinant vectors disclosed herein (for example, a recombinant AAVvector) can be used in several different therapeutic applications,depending on the protein of interest encoded by the recombinant vector.

In certain embodiments, the uses are for the treatment of hereditaryhemochromatosis (HH), a major disorder of iron overload, Wilson'sdisease, a genetic disorder of copper overload, and alpha1-antitrypsin(α1-AT) deficiency. In certain embodiments, the protein is humanAlpha1-antitrypsin (α1-AT, Accession: P01009.3), HFE protein (AccessionNP_000401.1 or Q30201), or hepatic protein ATP7B (Accession P35670.4) orvariants with greater than 50, 60, 70, 80, 90, 95, or 95 sequenceidentity or similarity.

In certain embodiments, the use is for the treatment ofhypercholesterolaemia using a promotor herein in operable combinationwith a nucleic acid that encodes for human phenylalanine hydroxylase(Accession: P00439.1) or variants with greater than 50, 60, 70, 80, 90,95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of Type 1tyrosinemia using a promotor herein in operable combination with anucleic acid that encodes for human fumarylacetoacetate hydrolase(Accession: P16930.2) or variants with greater than 50, 60, 70, 80, 90,95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of Type 2tyrosinemia using a promotor herein in operable combination with anucleic acid that encodes for human tyrosine aminotransferase(Accession: P17735.1) or variants with greater than 50, 60, 70, 80, 90,95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of homocystinuriaand hyperhomocysteinemia using a promotor herein in operable combinationwith a nucleic acid that encodes for human methylenetetrahydrofolatereductase (Accession: P42898.3) or variants with greater than 50, 60,70, 80, 90, 95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of hyperlipidemiaand hypercholesterolemia using a promotor herein in operable combinationwith a nucleic acid that encodes for human medium chain acyl-CoAdehydrogenase (Accession: P11310.1) or variants with greater than 50,60, 70, 80, 90, 95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of Galactosemiausing a promotor herein in operable combination with a nucleic acid thatencodes for human galactose-1-phosphate uridyl transferase (Accession:P07902.3) or variants with greater than 50, 60, 70, 80, 90, 95, or 95sequence identity or similarity.

In certain embodiments, the use is for the treatment of Lesch-Nyhansyndrome using a promotor herein in operable combination with a nucleicacid that encodes for human hypoxanthine phosphoribosyl-transferase(Accession: P00492.2) or variants with greater than 50, 60, 70, 80, 90,95, or 95 sequence identity or similarity.

In certain embodiments, the use is for the treatment of Gaucher diseaseusing a promotor herein in operable combination with a nucleic acid thatencodes for human cerebrosidase (Accession: P07602.2, Accession:P04062.3) or variants with greater than 50, 60, 70, 80, 90, 95, or 95sequence identity or similarity.

In certain embodiments, the use is for the treatment of Tay-Sachsdisease using a promotor herein in operable combination with a nucleicacid that encodes for human beta-hexosaminidase A (Accession: P06865.2)or variants with greater than 50, 60, 70, 80, 90, 95, or 95 sequenceidentity or similarity.

In certain embodiments, the use is for the treatment of Fabry diseaseusing a promotor in operable combination with a nucleic acid thatencodes for human α-galactosidase (Accession: P06280.1) or variants withgreater than 50, 60, 70, 80, 90, 95, or 95 sequence identity orsimilarity.

In certain embodiments, the use is for the treatment of Hunter syndromeusing a promotor in operable combination with a nucleic acid thatencodes for human iduronate sulphatase (Accession: P22304.1) or variantswith greater than 50, 60, 70, 80, 90, 95, or 95 sequence identity orsimilarity.

In certain embodiments, the use is for the treatment of glycogen storagedisease type Ia using a promotor in operable combination with a nucleicacid that encodes for human glucose-6-phosphatase (Accession: P35575.2)or variants with greater than 50, 60, 70, 80, 90, 95, or 95 sequenceidentity or similarity.

In certain embodiments, the use is for the treatment of ammoniametabolism using a promotor in operable combination with a nucleic acidthat encodes for human ornithine transcarbamylase (Accession: P00480.3)or variants with greater than 50, 60, 70, 80, 90, 95, or 95 sequenceidentity or similarity.

In certain embodiments, the use is for the treatment of phenylketonuriausing a promotor in operable combination with a nucleic acid thatencodes for human low-density lipoprotein receptor (Accession: P01130.1)or variants with greater than 50, 60, 70, 80, 90, 95, or 95 sequenceidentity or similarity.

In certain embodiments, the use is for the treatment of propionicacidemia using a promotor in operable combination with a nucleic acidthat encodes for human propionyl-coenzyme A carboxylase, either PCCAand/or PCCB (Accession: P05166.3 beta, NP_000273.2 alpha, NP_001121164.1alpha) or variants with greater than 50, 60, 70, 80, 90, 95, or 95sequence identity or similarity.

Also contemplated are uses in vaccine regimens, e.g., for co-delivery ofa cytokine, or for delivery of an immunogen or antigen.

Recombinant virus particles, capsids, or vectors comprising nucleicacids disclosed herein can be delivered to liver via the hepatic artery,the portal vein, or intravenously to yield therapeutic levels oftherapeutic proteins or clotting factors in the blood. The capsid orvector is preferably suspended in a physiologically compatible carrier,may be administered to a human or non-human mammalian patient. Suitablecarriers may be readily selected by one of skill in the art in view ofthe indication for which the transfer virus is directed. For example,one suitable carrier includes saline, which may be formulated with avariety of buffering solutions (e.g., phosphate buffered saline). Otherexemplary carriers include sterile saline, lactose, sucrose, calciumphosphate, gelatin, dextran, agar, pectin, sesame oil, and water.

Optionally, the compositions of the disclosure may contain otherpharmaceutically acceptable excipients, such as preservatives, orchemical stabilizers. Suitable exemplary preservatives includechlorobutanol, potassium sorbate, sorbic acid, sulfur dioxide, propylgallate, the parabens, ethyl vanillin, glycerin, phenol, andparachlorophenol. Suitable chemical stabilizers include gelatin andalbumin.

The recombinant virus particles, capsids, or vectors are administered insufficient amounts to transfect the cells and to provide sufficientlevels of gene transfer and expression to provide a therapeutic benefitwithout undue adverse effects, or with medically acceptablephysiological effects, which can be determined by those skilled in themedical arts. Conventional and pharmaceutically acceptable routes ofadministration include, but are not limited to, direct delivery to adesired organ (e.g., the liver (optionally via the hepatic artery) orlung), oral, inhalation, intranasal, intratracheal, intraarterial,intraocular, intravenous, intramuscular, subcutaneous, intradermal, andother parental routes of administration. Routes of administration may becombined, if desired.

Dosages of the recombinant virus particles, capsids, or vectors willdepend primarily on factors such as the condition being treated, theage, weight and health of the patient, and may thus vary among patients.For example, a therapeutically effective human dosage of the viralvector is generally in the range of from about 0.1 ml to about 100 ml ofsolution containing concentrations of from about 1×10⁹ to 1×10¹⁶ genomesvirus vector.

Other useful therapeutic proteins encoded by the nucleic acids (e.g.,operably in combination with promoters) reported herein include hormonesand growth and differentiation factors including, without limitation,insulin, glucagon, growth hormone (GH), parathyroid hormone (PTH),growth hormone releasing factor (GRF), follicle stimulating hormone(FSH), luteinizing hormone (LH), human chorionic gonadotropin (hCG),vascular endothelial growth factor (VEGF), angiopoietins, angiostatin,granulocyte colony stimulating factor (GCSF), erythropoietin (EPO),connective tissue growth factor (CTGF), basic fibroblast growth factor(bFGF), acidic fibroblast growth factor (aFGF), epidermal growth factor(EGF), platelet-derived growth factor (PDGF), insulin growth factors Iand II (IGF-I and IGF-II), any one of the transforming growth factoralpha superfamily, including TGFalpha, activins, inhibins, or any of thebone morphogenic proteins (BMP) BMPs 1-15, any one of theheregluin/neuregulin/ARIA/neu differentiation factor (NDF) family ofgrowth factors, nerve growth factor (NGF), brain-derived neurotrophicfactor (BDNF), neurotrophins NT-3 and NT-4/5, ciliary neurotrophicfactor (CNTF), glial cell line derived neurotrophic factor (GDNF),neurturin, agrin, any one of the family of semaphorins/collapsins,netrin-1 and netrin-2, hepatocyte growth factor (HGF), ephrins, noggin,sonic hedgehog and tyrosine hydroxylase.

Other therapeutic proteins encoded by the nucleic acids (e.g., operablyin combination with promoters) reported herein include those thatregulate the immune system including, without limitation, cytokines andlymphokines such as thrombopoietin (TPO), interleukins (IL) IL-1 throughIL-25 (including IL-2, IL-4, IL-12 and IL-18), monocyte chemoattractantprotein, leukemia inhibitory factor, granulocyte-macrophage colonystimulating factor, Fas ligand, tumor necrosis factors alpha and beta,interferons alpha, beta, and gamma, stem cell factor, flk-2/flt3 ligand.Proteins produced by the immune system are also useful. These include,without limitations, immunoglobulins IgG, IgM, IgA, IgD and IgE,chimeric immunoglobulins, humanized antibodies, single chain antibodies,T cell receptors, chimeric T cell receptors, single chain T cellreceptors, class I and class II MHC molecules, as well as engineeredimmunoglobulins and MHC molecules. Useful proteins also includecomplement regulatory proteins such as complement regulatory proteins,membrane cofactor protein (MCP), decay accelerating factor (DAF), CR1,CF2 and CD59.

Other therapeutic proteins encoded by the nucleic acids (e.g., operablyin combination with promoters) reported herein are receptors for thehormones, growth factors, cytokines, lymphokines, regulatory proteinsand immune system proteins. The disclosure encompasses receptors forcholesterol regulation and/or lipid modulation, including the lowdensity lipoprotein (LDL) receptor, high density lipoprotein (HDL)receptor, the very low density lipoprotein (VLDL) receptor, andscavenger receptors. The disclosure also encompasses proteins such asmembers of the steroid hormone receptor superfamily includingglucocorticoid receptors and estrogen receptors, Vitamin D receptors andother nuclear receptors. In addition, useful proteins includetranscription factors such as jun, fos, max, mad, serum response factor(SRF), AP-1, AP2, myb, MyoD and myogenin, ETS-box containing proteins,TFE3, E2F, ATF1, ATF2, ATF3, ATF4, ZFS, NFAT, CREB, HNF-4, C/EBP, SP1,CCAAT-box binding proteins, interferon regulation factor (IRF-1), Wilmstumor protein, ETS-binding protein, STAT, GATA-box binding proteins,e.g., GATA-3, and the forkhead family of winged helix proteins.

Other useful proteins include, carbamoyl synthetase I, ornithinetranscarbamylase, arginosuccinate synthetase, arginosuccinate lyase,arginase, fumarylacetacetate hydrolase, phenylalanine hydroxylase,alpha-1 antitrypsin, glucose-6-phosphatase, porphobilinogen deaminase,cystathione beta-synthase, branched chain ketoacid decarboxylase,albumin, isovaleryl-coA dehydrogenase, propionyl CoA carboxylase, methylmalonyl CoA mutase, glutaryl CoA dehydrogenase, insulin,beta-glucosidase, pyruvate carboxylate, hepatic phosphorylase,phosphorylase kinase, glycine decarboxylase, H-protein, T-protein, acystic fibrosis transmembrane regulator (CFTR) sequence, and adystrophin cDNA sequence. Still other useful proteins include enzymessuch as may be useful in enzyme replacement therapy, which is useful ina variety of conditions resulting from deficient activity of enzyme. Forexample, enzymes that contain mannose-6-phosphate may be utilized intherapies for lysosomal storage diseases (e.g., a suitable gene includesthat encoding beta-glucuronidase (GUSB)).

Other useful proteins include non-naturally occurring polypeptides, suchas chimeric or hybrid polypeptides having a non-naturally occurringamino acid sequence containing insertions, deletions or amino acidsubstitutions. For example, single-chain engineered immunoglobulinscould be useful in certain immunocompromised patients. Other types ofnon-naturally occurring gene sequences include antisense molecules andcatalytic nucleic acids, such as ribozymes, which could be used toreduce overexpression of a target.

Reduction and/or modulation of expression of a protein is particularlydesirable for treatment of hyperproliferative conditions characterizedby hyperproliferating cells, as are cancers and psoriasis. Targetpolypeptides include those polypeptides which are produced exclusivelyor at higher levels in hyperproliferative cells as compared to normalcells. Target antigens include polypeptides encoded by oncogenes such asmyb, myc, fyn, and the translocation gene bcr/abl, ras, src, P53, neu,trk and EGRF. In addition to oncogene products as target antigens,target polypeptides for anti-cancer treatments and protective regimensinclude variable regions of antibodies made by B cell lymphomas andvariable regions of T cell receptors of T cell lymphomas which, in someembodiments, are also used as target antigens for autoimmune disease.Other tumor-associated polypeptides can be used as target polypeptidessuch as polypeptides which are found at higher levels in tumor cellsincluding the polypeptide recognized by monoclonal antibody 17-1A andfolate binding polypeptides.

Other suitable therapeutic polypeptides and proteins include those whichmay be useful for treating individuals suffering from autoimmunediseases and disorders by conferring a broad based protective immuneresponse against targets that are associated with autoimmunity includingcell receptors and cells which produce “self”-directed antibodies. Tcell mediated autoimmune diseases include Rheumatoid arthritis (RA),multiple sclerosis (MS), Sjogren's syndrome, sarcoidosis, insulindependent diabetes mellitus (IDDM), autoimmune thyroiditis, reactivearthritis, ankylosing spondylitis, scleroderma, polymyositis,dermatomyositis, psoriasis, vasculitis, Wegener's granulomatosis,Crohn's disease and ulcerative colitis. Each of these diseases ischaracterized by T cell receptors (TCRs) that bind to endogenousantigens and initiate the inflammatory cascade associated withautoimmune diseases.

Vectors reported herein may be formulated in a manner which permits theexpression of a protein carried by the vectors to induce an immuneresponse to a selected antigen. For example, in order to promote animmune response, the antigen may be expressed from a promoter disclosedherein, the vector can be adjuvanted as described herein, and/or thevector can be put into degenerating tissue.

Examples of suitable immunogenic antigens include those selected from avariety of viral families Example of desirable viral families againstwhich an immune response would be desirable include, the picornavirusfamily, which includes the genera rhinoviruses, which are responsiblefor about 50% of cases of the common cold; the genera enteroviruses,which include polioviruses, coxsackieviruses, echoviruses, and humanenteroviruses such as hepatitis A virus; and the genera apthoviruses,which are responsible for foot and mouth diseases, primarily innon-human animals Within the picornavirus family of viruses, targetantigens include the VP1, VP2, VP3, VP4, and VPG. Other viral familiesinclude the astroviruses and the calcivirus family. The calcivirusfamily encompasses the Norwalk group of viruses, which are an importantcausative agent of epidemic gastroenteritis. Still another viral familydesirable for use in targeting antigens for inducing immune responses inhumans and non-human animals is the togavirus family, which includes thegenera alphavirus, which include Sindbis viruses, RossRiver virus, andVenezuelan, Eastern & Western Equine encephalitis, and rubivirus,including Rubella virus. The flaviviridae family includes dengue, yellowfever, Japanese encephalitis, St. Louis encephalitis and tick borneencephalitis viruses. Other target antigens may be generated from theHepatitis C or the coronavirus family, which includes a number ofnon-human viruses such as infectious bronchitis virus (poultry), porcinetransmissible gastroenteric virus (pig), porcine hemagglutinatinencephalomyelitis virus (pig), feline infectious peritonitis virus(cats), feline enteric coronavirus (cat), canine coronavirus (dog), andhuman respiratory coronaviruses, which may cause the common cold and/ornon-A, B or C hepatitis, and which include the putative cause of suddenacute respiratory syndrome (SARS). Within the coronavirus family, targetantigens include the E1 (also called M or matrix protein), E2 (alsocalled S or Spike protein), E3 (also called HE or hemagglutin-elterose)glycoprotein (not present in all coronaviruses), or N (nucleocapsid).Still other antigens may be targeted against the arterivirus family andthe rhabdovirus family. The rhabdovirus family includes the generavesiculovirus (e.g., Vesicular Stomatitis Virus), and the generallyssavirus (e.g., rabies). Within the rhabdovirus family, suitableantigens may be derived from the G protein or the N protein. The familyfiloviridae, which includes hemorrhagic fever viruses such as Marburgand Ebola virus may be a suitable source of antigens. The paramyxovirusfamily includes parainfluenza Virus Type 1, parainfluenza Virus Type 3,bovine parainfluenza Virus Type 3, rubulavirus (mumps virus,parainfluenza Virus Type 2, parainfluenza virus Type 4, Newcastledisease virus (chickens), rinderpest, morbillivirus, which includesmeasles and canine distemper, and pneumovirus, which includesrespiratory syncytial virus. The influenza virus is classified withinthe family orthomyxovirus and is a suitable source of antigen (e.g., theHA protein, the N1 protein). The bunyavirus family includes the generabunyavirus (California encephalitis, La Crosse), phlebovirus (RiftValley Fever), hantavirus (puremala is a hemahagin fever virus),nairovirus (Nairobi sheep disease) and various unassigned bungaviruses.The arenavirus family provides a source of antigens against LCM andLassa fever virus. Another source of antigens is the bornavirus family.The reovirus family includes the genera reovirus, rotavirus (whichcauses acute gastroenteritis in children), orbiviruses, and cultivirus(Colorado Tick fever, Lebombo (humans), equine encephalosis, bluetongue). The retrovirus family includes the sub-family oncorivirinalwhich encompasses such human and veterinary diseases as feline leukemiavirus, HTLVI and HTLVII, lentivirinal (which includes HIV, simianimmunodeficiency virus, feline immunodeficiency virus, equine infectiousanemia virus, and spumavirinal). The papovavirus family includes thesub-family polyomaviruses (BKU and JCU viruses) and the sub-familypapillomavirus (associated with cancers or malignant progression ofpapilloma). The adenovirus family includes viruses (EX, AD7, ARD, O.B.)which cause respiratory disease and/or enteritis. The parvovirus familyfeline parvovirus (feline enteritis), feline panleucopeniavirus, canineparvovirus, and porcine parvovirus. The herpesvirus family includes thesub-family alphaherpesvirinae, which encompasses the genera simplexvirus(HSVI, HSVII), varicellovirus (pseudorabies, varicella zoster) and thesub-family betaherpesvirinae, which includes the genera cytomegalovirus(HCMV, muromegalovirus) and the sub-family gamma herpesvirinae, whichincludes the genera lymphocryptovirus, EBV (Burkitts lymphoma), humanherpesviruses 6A, 6B and 7, Kaposi's sarcoma-associated herpesvirus andcercopithecine herpesvirus (B virus), infectious rhinotracheitis,Marek's disease virus, and rhadinovirus. The poxvirus family includesthe sub-family chordopoxvirinae, which encompasses the generaorthopoxvirus (Variola major (Smallpox) and Vaccinia (Cowpox)),parapoxvirus, avipoxvirus, capripoxvirus, leporipoxvirus, suipoxvirus,and the sub-family entomopoxvirinae. The hepadnavirus family includesthe Hepatitis B virus. One unclassified virus which may be suitablesource of antigens is the Hepatitis delta virus, Hepatitis E virus, andprions. Another virus which is a source of antigens is Nipan Virus.Still other viral sources may include avian infectious bursal diseasevirus and porcine respiratory and reproductive syndrome virus. Thealphavirus family includes equine arteritis virus and variousEncephalitis viruses.

The present disclosure may also encompass protein based immunogens whichare useful to immunize a human or non-human animal against otherpathogens including bacteria, fungi, parasitic microorganisms ormulticellular parasites which infect human and non-human vertebrates, orfrom a cancer cell or tumor cell. Examples of bacterial pathogensinclude pathogenic gram-positive cocci include pneumococci;staphylococci (and the toxins produced thereby, e.g., enterotoxin B);and streptococci. Pathogenic gram-negative cocci include meningococcus;gonococcus. Pathogenic enteric gram-negative bacilli includeenterobacteriaceae; pseudomonas, acinetobacteria and eikenella;melioidosis; salmonella; shigella; haemophilus; moraxella; H. ducreyi(which causes chancroid); brucella species (brucellosis); Francisellatularensis (which causes tularemia); Yersinia pestis (plague) and otherYersinia (pasteurella); streptobacillus moniliformis and spirillum;Gram-positive bacilli include Listeria monocytogenes; erysipelothrixrhusiopathiae; Corynebacterium diphtheria (diphtheria); cholera; B.anthracia (anthrax); donovanosis (granuloma inguinale); andbartonellosis. Diseases caused by pathogenic anaerobic bacteria includetetanus; botulism (Clostridum botulinum and its toxin); Clostridiumperfringens and its epsilon toxin; other clostridia; tuberculosis;leprosy; and other mycobacteria. Pathogenic spirochetal diseases includesyphilis; treponematoses: yaws, pinta and endemic syphilis; andleptospirosis. Other infections caused by higher pathogen bacteria andpathogenic fungi include glanders (Burkholderia mallei); actinomycosis;nocardiosis; cryptococcosis, blastomycosis, histoplasmosis andcoccidioidomycosis; candidiasis, aspergillosis, and mucormycosis;sporotrichosis; paracoccidiodomycosis, petriellidiosis, torulopsosis,mycetoma and chromomycosis; and dermatophytosis. Rickettsial infectionsinclude Typhus fever, Rocky Mountain spotted fever, Q fever (Coxiellaburnetti), and Rickettsial pox. Examples of mycoplasma and chlamydialinfections include: Mycoplasma pneumoniae; lymphogranuloma venereum;psittacosis; and perinatal chlamydial infections. Pathogenic eukaryotesencompass pathogenic protozoans and helminths and infections producedthereby include: amebiasis; malaria; leishmaniasis; trypanosomiasis;toxoplasmosis; Pneumocystis carinii; Trichans; Toxoplasma gondii;babesiosis; giardiasis; trichinosis; filariasis; schistosomiasis;nematodes; trematodes or flukes; and cestode (tapeworm) infections.

Many of these organisms and/or the toxins produced thereby have beenidentified by the Centers for Disease Control [(CDC), Department ofHealth and Human Services, USA], as agents which have potential for usein biological attacks. For example, some of these biological agents,include, Bacillus anthracia (anthrax), Clostridium botulinum and itstoxin (botulism), Yersinia pestis (plague), variola major (smallpox),Francisella tularensis (tularemia), and viral hemorrhagic fevers[filoviruses (e.g., Ebola, Marburg], and arenaviruses [e.g., Lassa,Machupo]), all of which are currently classified as Category A agents;Coxiella burnetti (Q fever); Brucella species (brucellosis),Burkholderia mallei (glanders), Burkholderia pseudomallei (meloidosis),Ricinus communis and its toxin (ricin toxin), Clostridium perfringensand its toxin (epsilon toxin), Staphylococcus species and their toxins(enterotoxin B), Chlamydia psittaci (psittacosis), water safety threats(e.g., Vibrio cholerae, Crytosporidium parvum), Typhus fever (Richettsiapowazekii), and viral encephalitis (alphaviruses, e.g., Venezuelanequine encephalitis; eastern equine encephalitis; western equineencephalitis); all of which are currently classified as Category Bagents; and Nipan virus and hantaviruses, which are currently classifiedas Category C agents. In addition, other organisms, which are soclassified or differently classified, may be identified and/or used forsuch a purpose in the future. It will be readily understood that theviral vectors and other constructs described herein are useful todeliver antigens from these organisms, viruses, their toxins or otherby-products, which will prevent and/or treat infection or other adversereactions with these biological agents.

In certain embodiments, a protein for expression in a vector of thedisclosure are a segment of a variable region of T cells eliciting animmune response, i.e., to eliminate cytotoxic T cells. In rheumatoidarthritis (RA), several specific variable regions of TCRs which areinvolved in the disease have been characterized. These TCRs include V-3,V-14, V-17 and V-17. Thus, delivery of a nucleic acid sequence thatencodes at least one of these polypeptides will elicit an immuneresponse that will target T cells involved in RA. In multiple sclerosis(MS), several specific variable regions of TCRs which are involved inthe disease have been characterized. These TCRs include V-7 and V-10.Thus, delivery of a nucleic acid sequence that encodes at least one ofthese polypeptides will elicit an immune response that will target Tcells involved in MS. In scleroderma, several specific variable regionsof TCRs which are involved in the disease have been characterized. TheseTCRs include V-6, V-8, V-14 and V-16, V-3C, V-7, V-14, V-15, V-16, V-28and V-12. Thus, delivery of a nucleic acid molecule that encodes atleast one of these polypeptides will elicit an immune response that willtarget T cells involved in scleroderma.

Recombinant viral vectors of the disclosure provides an efficient genetransfer vehicle which can deliver a selected proteins to a selectedhost cell in vivo or ex vivo even where the organism has neutralizingantibodies to the protein. In one embodiment, the vectors disclosedherein and the cells are mixed ex vivo; the infected cells are culturedusing conventional methodologies; and the transduced cells arere-infused into the patient.

Additional Embodiments

In certain embodiments, the disclosure relates to recombinant viralvectors comprising a liver specific promotor nucleic acid sequence inoperable combination with a heterologous nucleic acid sequence encodinga protein. Typically, the nucleic acid sequence encoding the proteincomprises a higher percentage of liver cell specific amino acid codonscompared to overall human codon usage. In certain embodiments, thedisclosure relates to methods of treating a subject diagnosed with agenetic trait that results in expression of a mutated or truncatednon-functional protein by administering an effective amount of a vectordisclosed herein configured to express a functional protein from theliver.

In certain embodiments, the vector comprises a viral nucleic acidsequence of greater than 10, 20, 30, 40, 50, 100, or 200 nucleotides. Incertain embodiments, the viral nucleic acid sequence is a segment ofhuman adeno-associated virus (hAAV) of serotypes 1, 2, 3B, 4, 5, 6, 7,8, 9 or combinations or variants thereof, typically comprising an AAVinverted terminal repeat.

In certain embodiments, the disclosure relates to a viral particle,e.g., capsid comprising a vector disclosed herein, e.g., the vectorpackaged in a capsid. The capsid may be a recombinant or chimericparticle or capsid, e.g., capsid having amino acid sequences that are acombination of AAV pseudotypes for VP 1, 2, or 3. An AAV capsid VP maybe derived from a human gene or animal AAV gene, or combinations withgenetically engineered alterations, i.e., AAV isolated from infectedhuman cells or a non-human primate Animal AAV include those derived fromavian, bovine, porcine, mice, etc. In certain embodiments, the capsidmay have amino acid sequences that are bioengineered or syntheticcapsids identified through methods such as directed evolution orrational design.

In certain embodiments, vectors disclosed herein are a single or doublestranded nucleic acid or self-complementary nucleic acid of less than5.1, 5.0, 4.9, 4.8, 4.7, 4.6, or 4.5 kb of nucleotides in total. Incertain embodiments, the vector is replication-incompetent inside ahuman host, e.g., vector does not encode a viral polymerase.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to

(SEQ ID NO: 21) GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTA (SEQ ID NO: 43)ATAATCTCAGGACAAACA and/or (SEQ ID NO: 20)TATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC.

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 21between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 21 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides. In certain embodiments, the liverspecific promotor sequence comprises a sequence having at least 50, 60,70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequence identity to SEQ IDNO: 4, 5, 6, or 7.

As used herein, the liver specific promotor refers to the sequences inthe 5′ direction of the transcriptional start site of the protein to beproduced. Promotor sequences disclosed herein may contain combinationsof other known promotors, enhancers, other sequences, and fragmentsthereof. For example, SEQ ID NO: 21 is the sequence of the shortened ABPenhancer. By itself it does not function as a promoter, it serves toenhance the expression conferred by the core promoter, SEQ ID NO: 20,SynO, which by itself does not confer efficient gene expression.Additional enhancer sequences which may replace or augment the short ABPenhancer are contemplated.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to CGGAGGAGCAAACAGGG (SEQ ID NO: 97) and/orTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC (SEQ ID NO: 20).

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 97between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 97 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to

(SEQ ID NO: 98) CGGAGGAGCAAACAGGGGCTAAGTCCAC and/or (SEQ ID NO: 20)TATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC.

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 98between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 98 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to

(SEQ ID NO: 99) GGCTGCTGGTGAATATTAACCAAGGTC and/or (SEQ ID NO: 20)TATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC.

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 99between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 99 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to

(SEQ ID NO: 100) GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGAGCAAACAGGGGCTAAGTCCAC and/or (SEQ ID NO: 20)TATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC.

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 100between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 100 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to

(SEQ ID NO: 101) GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGAGCAAACAGGGACTAAGTCCAC and/or (SEQ ID NO: 20)TATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC.

In certain embodiments, SEQ ID NO 20 is 3′ or after SEQ ID NO: 101between a nucleotide linker, e.g., connected with a linker asillustrated: 5′-SEQ ID NO: 101 followed by a linker followed by SEQ IDNO: 20-3′. The linker may be between 0 to 200 nucleotides, 10 to 100nucleotides, 20 to 70 nucleotides, 30 to 60 nucleotides, 30 to 40nucleotides, 32 to 36 nucleotides.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to SEQ ID NO: 4, 5, 6, 7, 102, 103, 104, 105,106, 107, or 108.

In certain embodiments, liver specific promotor nucleic acid sequence isof less than 205 or 250 nucleotides. The terms “less than 205 or 250nucleotides” refers to the length of a single strand or the length ofdouble stranded base pairs. The functional promoter is double strandedafter intracellular conversion following viral infection. It would notfunction if it were single stranded.

In certain embodiments, the disclosure contemplates the first nucleotideof the promotor sequence is the 5′ “G” in the HFN1a TF binding site,GTTAAT (SEQ ID NO: 25), e.g., promotor is 5′-SEQ ID NO: 21 which isfollowed by a linker and further followed by a transcriptional startsite (TSS), e.g. TCATCCTC (SEQ ID NO: 109), wherein the last nucleotidein the transcriptional start site is the end of the promotor sequence.In certain embodiments the linker comprises a TATAA (SEQ ID NO: 26) boxand a GC rich spacer. In certain embodiments, the disclosurecontemplates the first nucleotide of the promotor sequence is a 5′ “G”in GTTAA (SEQ ID NO: 27), GTTA (SEQ ID NO: 28), GTT (SEQ ID NO: 29). Incertain embodiments, the first nucleotide of the promotor sequence is a5′ “T” in TTAAT (SEQ ID NO: 30), TTAA (SEQ ID NO: 31), TTA (SEQ ID NO:32). In certain embodiments, the first nucleotide of the promotorsequence is a 5′ “A” in AAT (SEQ ID NO: 33).

In certain embodiments, the disclosure contemplates a promotorcomprising 5′-SEQ ID NO: 21 or 97 or 98 or 99 or 100 or 101 optionallyfollowed by a linker, followed by a TATAA box, followed by a GC richspacer followed by and a transcriptional start site. In certainembodiments, the GC rich spacer is a sequence wherein greater than 60,70, 80, or 90% of the nucleotides are G or C, e.g., over a window of 5to 35 nucleotide, 10 to 30 nucleotides, or 15 to 40 nucleotide, or 5 to50 or 60 nucleotides. In certain embodiments, the CG rich spacer isGGCCAGCAGCAGCCTGACCACATC (SEQ ID NO: 110). In certain embodiments, theliver specific promotor sequence comprises a sequence having at least50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequence identity toSEQ ID NO: 110.

In certain embodiments, the liver specific promotor sequence comprises asequence having at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or100% sequence identity to one of:

SEQ ID NO: 34: GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 35:TTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGAC AAACA; SEQ ID NO: 36:TAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA AACA; SEQ ID NO: 37:AATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAA ACA; SEQ ID NO: 38:ATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAA CA; SEQ ID NO: 39:TTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAAC A; SEQ ID NO: 40:TTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAAC A; SEQ ID NO: 41:TTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 42:TTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 44:TGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 45:GTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 46:TGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 47:GCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 48:CCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 49:CCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 50:CTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACA; SEQ ID NO: 51:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAAAC; SEQ ID NO: 52:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAAA; SEQ ID NO: 53:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAA; SEQ ID NO: 54:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAA; SEQ ID NO: 55:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CA; SEQ ID NO: 56:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA C; SEQ ID NO: 57:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGG A; SEQ ID NO: 58:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGG; SEQ ID NO: 59:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAG; SEQ ID NO: 60:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCA; SEQ ID NO: 61:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTC; SEQ ID NO: 62:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCT; SEQ ID NO: 63:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATC; SEQ ID NO: 64:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAAT; SEQ ID NO: 65:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAA; SEQ ID NO: 66:GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAAAC; SEQ ID NO: 67:TTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGAC AAA; SEQ ID NO: 68:TAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA A; SEQ ID NO: 69:AATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA; SEQ ID NO: 70:ATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGAC; SEQ ID NO: 71:TTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA; SEQ ID NO: 72:TTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGG; SEQ ID NO: 73:TTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAG; SEQ ID NO: 74:TTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCA; SEQ ID NO: 75:TGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTC; SEQ ID NO: 76:GTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCT; SEQ ID NO: 77:TGGCCCTTGCGATGTTTGCTCTGGTTAATAATC; SEQ ID NO: 78:GCCCTTGCGATGTTTGCTCTGGTTAATAAT; SEQ ID NO: 79:CCCTTGCGATGTTTGCTCTGGTTAATAA; SEQ ID NO: 80: CCTTGCGATGTTTGCTCTGGTTAATA;SEQ ID NO: 81: CTTGCGATGTTTGCTCTGGTTAAT; SEQ ID NO: 82:TTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGAC AAAC; SEQ ID NO: 83:TAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA AA; SEQ ID NO: 84:AATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA A; SEQ ID NO: 85:ATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAA; SEQ ID NO: 86:TTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACA; SEQ ID NO: 87:TTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGAC; SEQ ID NO: 88:TTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA; SEQ ID NO: 89:TTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGG; SEQ ID NO: 90:TGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAG; SEQ ID NO: 91:TGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCA; SEQ ID NO: 92:GGCCCTTGCGATGTTTGCTCTGGTTAATAATCTC; SEQ ID NO: 93:GCCCTTGCGATGTTTGCTCTGGTTAATAATCT; SEQ ID NO: 94:CCCTTGCGATGTTTGCTCTGGTTAATAATC; SEQ ID NO: 95:CCTTGCGATGTTTGCTCTGGTTAATAAT; or SEQ ID NO: 96:CTTGCGATGTTTGCTCTGGTTAATAA.

In certain embodiments, the promotor may start with the first 5′nucleotide of SEQ ID NO: 34-96, and end with the last nucleotide of theTSS.

In certain embodiments, the protein is a fVIII or fIX or variantthereof. In certain embodiments, the promoter and codon optimizationschemes disclosed herein could be used for any liver-directed AAV genetherapies. Other metabolic diseases caused by deficiencies of liverenzymes and expression of those functional proteins are contemplated.

In certain embodiments, fVIII variant comprises an A1 domain, an A2domain, a RHQR sequence (SEQ ID NO: 24), an A3 domain, a C1 domain, anda C2 domain. In certain embodiments, the fVIII variant comprises adeleted B domain.

In certain embodiments, the fVIII variant comprises a linker of betweentwo and fifty, or two and twenty five, or two and fifteen amino acidsbetween the A2 domain and the A3 domain.

In certain embodiments, fVIII variant comprises an A1 domain, an A2domain, an activation peptide (ap) domain, an A3 domain, a C1 domain,and a C2 domain. In certain embodiments, the fVIII variant comprises adeleted B domain.

In certain embodiments, the fVIII variant comprises a linker of betweentwo and fifty, or two and twenty five, or two and fifteen amino acidsbetween the A2 domain and the an activation peptide (ap) domain.

In certain embodiments, the fVIII variant comprises a sequence having atleast 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequenceidentity to SEQ ID NO: 3.

In certain embodiments, the fVIII variant comprises a sequence having atleast 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequenceidentity to SEQ ID NO: 13, 14, 15, or 16.

In certain embodiments, the disclosure relates to methods wherein codonusage of a gene is adjusted according to the tissue it will beexpressed, e.g., liver tissue. In certain embodiments, the nucleic acidsequence encoding a protein comprises codons that are differentiallyutilized or represented in genes highly expressed within the liver orother specific tissue compared to the codon usage of the entire codingregion of the human genome and avoids codons that are under-representedin the liver or other specific tissue.

In certain embodiments, the nucleic acid sequence encoding the proteincomprises codons for greater than 50, 60, 70, 80, 90, or 95% or 100% ofthe amino acids that are preferred as provided in FIG. 2.

In certain embodiments, the nucleic acid sequence encoding a proteincomprises a higher percentage of liver cell specific amino acid codonscompared to overall human codon usage is a sequence having at least 50,60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequence identity to SEQID NO: 1.

In certain embodiments, fiX variant comprises a sequence having at least50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequence identity toSEQ ID NO: 17, 18, or 19.

In certain embodiments, the nucleic acid sequence encoding a proteincomprising a higher percentage of liver cell specific amino acid codonscompared to overall human codon usage is a sequence having at least 50,60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or 100% sequence identity to SEQID NO: 8, 9, or 10.

In certain embodiments, the nucleic acid sequence encoding the proteincomprises at least one of a) to g) wherein,

a) a ATC codon is in greater than 50% or 52% for Ile;

b) a ACC codon is in greater than 38% or 40% for Thr;

c) a TTC codon is in greater than 57% or 59% for Phe;

d) a GAG codon is in greater than 60% or 62% for Glu;

e) a CTG codon is in greater than 43% or 45% for Leu;

f) a AAG codon is in greater than 60% or 62% for Lys; and/or

g) a GAC codon is in greater than 56% or 58% for Asp.

In certain embodiments, the nucleic acid sequence encoding the proteincomprises at least two or more, or three or more, or four or more, fiveor more, six or more, or all of a), b), c), d), e), f) and g).

In certain embodiments, the nucleic acid sequence encoding the proteincomprises less than 100, 50, 30, 25, 20, 15, 10, 9, 8, 7, 6, 5, 4, 3, 2or no 5′-CG-3′ dinucleotides.

In certain embodiments, the disclosure relates to pharmaceuticalcompositions comprising a vector or a capsid as disclosed herein and apharmaceutically acceptable excipient.

In certain embodiments, the disclosure relates to methods of inducingblood clotting comprising administering an effective amount of a virusparticle, capsid, or vector as disclosed herein to a subject in needthereof.

In certain embodiments, the subject is diagnosed with hemophilia A or Bor acquired hemophilia or unlikely to respond to exogenous fVIIIinfusions.

In certain embodiments, the vector, virus particle, or capsid isadministered in combination with an immunosuppressive agent, e.g.,ciclosporin, tacrolimus, sirolimus, cyclophosphamide, methotrexate,azathioprine, mercaptopurine, fluorouracil, mycophenolic acid,dactinomycin, fingolimod, T-cell receptor antibody or binding protein,muromonab-CD3, IL-2 receptor antibody or binding protein, basiliximab,daclizumab, recombinant IFN-beta, TNF-alpha antibody or binding protein,infliximab, etanercept, adalimumab, or combinations thereof.

In certain embodiments, the disclosure relates to expression systemscomprising nucleic acids or vectors comprising nucleic acids disclosedherein.

In certain embodiments, the disclosure relates to expression systemscomprising nucleic acids or vectors comprising nucleic acids disclosedherein.

Additional embodiments are illustrated by the following clauses:

Clause 1. A vector comprising a liver specific promotor nucleic acidsequence of less than 250 nucleotides in operable combination with aheterologous nucleic acid sequence encoding a protein.

Clause 2. The vector of clause 1, wherein the liver specific promotorsequence comprises a sequence having greater than 50, 60, 70, 80, 85,90, 95, 96, 97, 98, or 99% sequence identity to

(SEQ ID NO: 110) GGCCAGCAGCAGCCTGACCACATC.

Clause 3. The vector of clause 1, wherein the liver specific promotorsequence comprises a sequence having greater than 50, 60, 70, 80, 85,90, 95, 96, 97, 98, or 99% sequence identity to SEQ ID NO: 4, 5, 6, 7,102, 103, 104, 105, 106, 107, or 108.

Clause 4. The vector of clause 1, wherein the protein is a fVIII or flXor variant thereof.

Clause 5. The vector of clause 4, wherein fVIII variant comprises an A1domain, an A2 domain, an ap domain, an A3 domain, a C1 domain, and a C2domain

Clause 6. The vector of clause 4, wherein the fVIII variant comprising adeleted B domain Clause 7. The vector of clause 4, wherein the fVIIIvariant comprises a linker of between two and fifty, or two and twentyfive, or two and fifteen amino acids between the A2 domain and the anactivation peptide(ap) domain.

Clause 8. The vector of clause 4, wherein the fVIII variant comprises asequence having greater than 50, 60, 70, 80, 85, 90, 91, 92, 93, 94, 95,96, 97, 98, or 99% sequence identity to SEQ ID NO: 3.

Clause 9. The vector of clause 4, wherein the fVIII variant comprises asequence having greater than 50, 60, 70, 80, 85, 90, 91, 92, 93, 94, 95,96, 97, 98, or 99% sequence identity to SEQ ID NO: 13, 14, 15, or 16.

Clause 10. The method of clause 1 wherein the heterologous nucleic acidssequence comprises a higher percentage of liver cell specific amino acidcodons compared to overall human codon usage.

Clause 11. The vector of clause 1, wherein the nucleic acid sequenceencoding a protein comprising a higher percentage of liver cell specificamino acid codons compared to overall human codon usage is a sequencehaving greater than 70, 80, 85, 90, 95, 96, 97, 98, or 99% sequenceidentity to SEQ ID NO: 2 or 11.

Clause 12. The vector of clause 3, wherein flX variant comprises asequence having greater than 50, 60, 70, 80, 85, 90, 91, 92, 93, 94, 95,96, 97, 98, or 99% sequence identity to SEQ ID NO: 17, 18, or 19.

Clause 13. The vector of clause 1, wherein the nucleic acid sequenceencoding a protein comprising a higher percentage of liver cell specificamino acid codons compared to overall human codon usage is a sequencehaving greater than 70, 80, 85, 90, 95, 96, 97, 98, or 99% sequenceidentity to SEQ ID NO: 8, 9, or 10.

Clause 14. A pharmaceutical composition comprising a vector of clause 1and a pharmaceutically acceptable excipient.

Clause 15. A method of inducing blood clotting comprising administeringan effective amount of a vector of clause 1 to a subject in needthereof.

Clause 16. The method of clause 15, wherein the subject is diagnosedwith hemophilia A or B or acquired hemophilia.

Clause 17. The method of clause 15, wherein the vector is administeredin combination with an immunosuppressive agent.

Clause 18. The method of clause 17, wherein the immunosuppressive agentis ciclosporin, tacrolimus, sirolimus, cyclophosphamide, methotrexate,azathioprine, mercaptopurine, fluorouracil, mycophenolic acid,dactinomycin, fingolimod, T-cell receptor antibody or binding protein,muromonab-CD3, IL-2 receptor antibody or binding protein, basiliximab,daclizumab, recombinant IFN-beta, TNF-alpha antibody or binding protein,infliximab, etanercept, or adalimumab.

The following examples are provided to illustrate certain particularfeatures and/or embodiments. These examples should not be construed tolimit the disclosure to the particular features or embodimentsdescribed.

EXAMPLES Example 1 Optimization of Clotting Factors and their EncodingDNA

This example illustrates the optimization of the coding sequences forfVIII and flX proteins to improve their utility for in vivo expressionand gene therapy.

The cDNA nucleotide sequence coding for fVIII and flX was initiallyoptimized by implementing a codon usage bias specific for the humanliver cell as compared to naturally occurring nucleotide sequence codingfor the corresponding non-codon optimized sequence for a human.

The adaptiveness of a nucleotide sequence encoding fVIII to the codonusage of human liver cells may be expressed as liver codon adaptationindex (LCAI). A codon adaptation index is defined as a measurement ofthe relative adaptiveness of the codon usage of a gene towards the codonusage of genes highly expressed in the human liver. The relativeadaptiveness of each codon is the ratio of the usage of each codon, tothat of the most abundant codon for the same amino acid. The CAI isdefined as the geometric mean of these relative adaptiveness values.Non-synonymous codons and termination codons (dependent on genetic code)are excluded. CAI values range from 0 to 1, with higher valuesindicating a higher proportion of the most abundant codons. Using thesequences of 43 highly expressed genes in the human liver, a customcodon-usage bias table specific for the human liver was constructed (seeFIG. 2A) that differs substantially from the most prevalent codons usedin total human coding sequences (FIG. 2B). Optimized coding sequence ofthe ET3 and HSQ variants of fVIII was developed with the moststatistically prevalent codons identified by the liver-usage biasanalysis.

ET3 is a B domain deleted (BDD) fVIII hybrid that contains human andporcine domains, i.e., sequence (A1 and A3 porcine, see FIGS. 1A and 1B)with a linker in the deleted B domain ET3 utilizes a 24 amino acidporcine sequence-derived OL linker sequence, i.e., porcine-derivedsequence

(SEQ ID NO: 23) SFAQNSRPPSASAPKPPVLRRHQR.The ET3 amino acid sequence is SEQ ID NO: 123:MQLELSTCVFLCLLPLGFSAIRRYYLGAVELSWDYRQSELLRELHVDTRFPATAPGALPLGPSVLYKKTVFVEFTDQLFSVARPRPPWMGLLGPTIQAEVYDTVVVTLKNMASHPVSLHAVGVSFWKSSEGAEYEDHTSQREKEDDKVLPGKSQTYVWQVLKENGPTASDPPCLTYSYLSHVDLVKDLNSGLIGALLVCREGSLTRERTQNLHEFVLLFAVFDEGKSWHSARNDSWTRAMDPAPARAQPAMHTVNGYVNRSLPGLIGCHKKSVYWHVIGMGTSPEVHSIFLEGHTFLVRHHRQASLEISPLTFLTAQTFLMDLGQFLLFCHISSHHHGGMEAHVRVESCAEEPQLRRKADEEEDYDDNLYDSDMDVVRLDGDDVSPFIQIRSVAKKHPKTWVHYIAAEEEDWDYAPLVLAPDDRSYKSQYLNNGPQRIGRKYKKVRFMAYTDETFKTREAIQHESGILGPLLYGEVGDTLLIIFKNQASRPYNIYPHGITDVRPLYSRRLPKGVKHLKDFPILPGEIFKYKWTVTVEDGPTKSDPRCLTRYYSSFVNMERDLASGLIGPLLICYKESVDQRGNQIMSDKRNVILFSVFDENRSWYLTENIQRFLPNPAGVQLEDPEFQASNIMHSINGYVFDSLQLSVCLHEVAYWYILSIGAQTDFLSVFFSGYTFKHKMVYEDTLTLFPFSGETVFMSMENPGLWILGCHNSDFRNRGMTALLKVSSCDKNTGDYYEDSYEDISAYLLSKNNAIEPRSFAQNSRPPSASAPKPPVLRRHQRDISLPTFQPEEDKMDYDDIFSTETKGEDFDIYGEDENQDPRSFQKRTRHYFIAAVEQLWDYGMSESPRALRNRAQNGEVPRFKKVVFREFADGSFTQPSYRGELNKHLGLLGPYIRAEVEDNIMVTFKNQASRPYSFYSSLISYPDDQEQGAEPRHNFVQPNETRTYFWKVQHHMAPTEDEFDCKAWAYFSDVDLEKDVHSGLIGPLLICRANTLNAAHGRQVTVQEFALFFTIFDETKSWYFTENVERNCRAPCHLQMEDPTLKENYRFHAINGYVMDTLPGLVMAQNQRIRWYLLSMGSNENIHSIHFSGHVFSVRKKEEYKMAVYNLYPGVFETVEMLPSKVGIWRIECLIGEHLQAGMSTTFLVYSKKCQTPLGMASGHIRDFQITASGQYGQWAPKLARLHYSGSINAWSTKEPFSWIKVDLLAPMIIHGIKTQGARQKFSSLYISQFIIMYSLDGKKWQTYRGNSTGTLMVFFGNVDSSGIKHNIFNPPIIARYIRLHPTHYSIRSTLRMELMGCDLNSCSMPLGMESKAISDAQITASSYFTNMFATWSPSKARLHLQGRSNAWRPQVNNPKEWLQVDFQKTMKVTGVTTQGVKSLLTSMYVKEFLISSSQDGHQWTLFFQNGKVKVFQGNQDSFTPVVNSLDPPLLTRYLRIHPQSWVHQIALRMEVLGCEAQDLYHSQ is a human fVIII variant wherein the BDD human fVIII protein issubstituted with a 14 amino acid human-derived SQ linker (SEQ ID NO: 22)SFSQNPPVLKRHQR. The HSQ amino acid sequence is SEQ ID NO: 3:MQIELSTCFELCLLRFCFSATRRYYLGAVELSWDYMQSDLGELPVDARFPPRVPKSFPENTSVVYKKTLFVEFTVHLFNIAKPRPPWMGLLGPTIQAEVYDTVVITLKNMASHPVSLHAVGVSYWKASEGAEYDDQTSQREKEDDKVFPGGSHTYVWQVLKENGPMASDPLCLTYSYLSHVDLVKDLNSGLIGALLVCREGSLAKEKTQTLHKFILLFAVFDEGKSWHSETKNSLMQDRDAASARAWPKMHTVNGYVNRSLPGLIGCHRKSVYWHVIGMGTTPEVHSIFLEGHTFLVRNHRQASLEISPITFLTAQTLLMDLGQFLLFCHISSHQHDGMEAYVKVDSCPEEPQLRMKNNEEAEDYDDDLTDSEMDVVRFDDDNSPSFIQIRSVAKKHPKTWVHYIAAEEEDWDYAPLVLAPDDRSYKSQYLNNGPQRIGRKYKKVREMAYTDETEKTREAIQHESGILGPLLYGEVGDTLLIIFKNQASRPYNIYPHGITDVRPLYSRRLPKGVKHLKDFPILPGEIFKYKWTVTVEDGPTKSDPRCLTRYYSSFVNMERDLASGLIGPLLICYKESVDQRGNQIMSDKRNVILFSVFDENRSWYLTENIQRFLPNPAGVQLEDPEFQASNIMHSINGYVFDSLQLSVCLHEVAYWYILSIGAQTDFLSVFFSGYTFKHKMVYEDTLTLFPFSGETVFMSMENPGLWILGCHNSDFRNRGMTALLKVSSCDKNTGDYYEDSYEDISAYLLSKNNAIEPRSFSQNPPVLKRHQREITRTTLQSDQEEIDYDDTISVEMKKEDFDIYDEDENQSPRSFQKKTRHYFIAAVERLWDYGMSSSPHVLRNRAQSGSVPQFKKVVFQEFTDGSFTQPLYRGELNEHLGLLGPYIRAEVEDNIMVTFRNQASRPYSFYSSLISYEEDQRQGAEPRKNFVKPNETKTYFWKVQHHMAPTKDEFDCKAWAYFSDVDLEKDVHSGLIGPLLVCHTNTLNPAHGRQVTVQEFALFFTIFDETKSWYFTENMERNCRAPCNIQMEDPTEKENYRFHAINGYIMDTLPGLVMAQDQRIRWYLLSMGSNENIHSIHESGHVFTVRKKEEYKMALYNLYPGVFETVEMLPSKAGIWRVECLIGEHLHAGMSTLFLVYSNKCQTPLGMASGHIRDFQITASGQYGQWAPKLARLHYSGSINAWSTKEPFSWIKVDLLAPMIIHGIKTQGARQKFSSLYISQFIIMYSLDGKKWQTYRGNSTGTLMVFFGNVDSSGIKHNIFNPPIIARYIRLHPTHYSIRSTLRMELMGCDLNSCSMPLGMESKAISDAQITASSYFTNMFATWSPSKARLHLQGRSNAWRPQVNNPKEWLQVDFQKTMKVTGVTTQGVKSLLTSMYVKEFLISSSQDGHQWTLFFQNGKVKVFQGNQDSFTPVVNSLDPPLLTRYLRIHPQSWVHQIALRMEVLGCEAQDLYBoth HSQ and ET3 contain the RHQR (SEQ ID NO: 24) recognition sequence forPACE/furin processing sequence for the B-domainThe liver codon optimized ET3 sequence is (SEQ ID NO: 12)ATGCAGCTGGAACTGTCTACCTGTGTGTTTCTGTGTCTGCTGCCTCTGGGGTTTTCTGCTATCCGCCGCTACTATCTGGGAGCCGTGGAGCTGTCCTGGGACTACAGGCAGAGCGAGCTGCTGAGAGAACTGCACGTGGATACCAGATTCCCAGCTACCGCTCCAGGAGCTCTGCCTCTGGGCCCATCCGTGCTGTACAAGAAAACCGTCTTCGTGGAGTTTACCGACCAGCTGTTCAGCGTGGCCAGGCCAAGACCACCTTGGATGGGACTGCTGGGACCAACCATCCAGGCTGAGGTGTACGATACCGTGGTCGTGACCCTGAAAAACATGGCCTCCCATCCCGTGAGCCTGCACGCTGTCGGGGTGTCCTTCTGGAAGTCCAGCGAGGGAGCCGAGTACGAAGACCATACCTCCCAGCGCGAGAAAGAAGACGATAAGGTGCTGCCTGGCAAAAGCCAGACCTATGTCTGGCAGGTGCTGAAGGAGAACGGACCAACCGCTAGCGACCCACCATGCCTGACCTACTCTTATCTGTCCCACGTCGATCTGGTGAAGGACCTGAATTCCGGACTGATCGGAGCTCTGCTGGTGTGTAGAGAGGGAAGCCTGACCAGAGAAAGAACCCAGAACCTGCATGAGTTCGTCCTGCTGTTCGCCGTGTTTGACGAAGGGAAGAGCTGGCACTCTGCCCGCAATGACTCCTGGACCAGAGCTATGGATCCAGCTCCTGCTAGAGCTCAGCCTGCTATGCACACCGTCAACGGCTACGTGAATCGGTCTCTGCCAGGACTGATCGGCTGCCATAAGAAAAGCGTCTATTGGCACGTGATCGGAATGGGCACCAGCCCCGAGGTGCATTCTATCTTCCTGGAAGGCCACACCTTTCTGGTCAGGCACCATAGACAGGCCTCTCTGGAGATCTCCCCTCTGACCTTCCTGACCGCTCAGACCTTTCTGATGGACCTGGGGCAGTTCCTGCTGTTTTGCCATATCTCTTCCCACCATCACGGAGGAATGGAGGCTCACGTCAGGGTGGAATCCTGTGCTGAGGAACCACAGCTGAGAAGAAAGGCTGATGAGGAAGAGGACTACGACGATAACCTGTATGACAGCGATATGGACGTCGTGCGCCTGGACGGCGACGATGTCAGCCCTTTCATCCAGATCCGGTCTGTGGCCAAGAAACATCCAAAGACCTGGGTCCACTACATCGCCGCTGAAGAGGAAGATTGGGACTATGCCCCCCTGGTGCTGGCTCCTGACGATAGATCCTACAAAAGCCAGTATCTGAACAATGGGCCCCAGCGCATCGGACGGAAGTACAAGAAAGTGAGGTTCATGGCCTATACCGACGAGACCTTTAAGACCAGAGAGGCTATCCAGCACGAATCCGGGATCCTGGGACCTCTGCTGTACGGCGAAGTGGGGGATACCCTGCTGATCATCTTCAAGAACCAGGCCTCCAGGCCATACAATATCTATCCCCATGGCATCACCGACGTGAGACCACTGTACAGCAGGAGACTGCCCAAGGGGGTCAAACACCTGAAGGATTTCCCCATCCTGCCTGGAGAGATCTTTAAGTATAAATGGACCGTCACCGTGGAAGACGGGCCTACCAAGTCCGATCCACGCTGCCTGACCCGGTACTATAGCTCTTTCGTGAACATGGAGAGAGACCTGGCTAGCGGACTGATCGGACCCCTGCTGATCTGTTACAAAGAGAGCGTGGACCAGAGGGGCAACCAGATCATGTCTGATAAGAGAAATGTCATCCTGTTCTCCGTGTTTGACGAGAACCGCAGCTGGTACCTGACCGAGAACATCCAGCGGTTCCTGCCAAATCCAGCTGGAGTGCAGCTGGAGGACCCAGAATTTCAGGCTTCCAACATCATGCATAGCATCAATGGCTACGTGTTCGATAGCCTGCAGCTGTCTGTCTGCCTGCACGAGGTGGCCTACTGGTATATCCTGTCCATCGGCGCTCAGACCGACTTCCTGTCCGTGTTCTTTAGCGGGTACACCTTTAAGCATAAAATGGTGTATGAGGATACCCTGACCCTGTTCCCCTTTTCTGGCGAGACCGTGTTCATGTCCATGGAAAACCCTGGCCTGTGGATCCTGGGGTGCCACAACAGCGACTTCAGGAATAGAGGAATGACCGCCCTGCTGAAAGTGTCCAGCTGTGATAAGAATACCGGCGATTACTATGAGGACTCTTACGAAGATATCTCCGCTTATCTGCTGAGCAAGAACAATGCCATCGAGCCCAGGTCTTTCGCTCAGAACTCCAGACCTCCAAGCGCTTCTGCTCCTAAGCCACCTGTGCTGAGAAGACATCAGAGGGACATCTCCCTGCCTACCTTCCAGCCAGAGGAAGATAAAATGGACTACGACGATATCTTCAGCACCGAGACCAAGGGGGAAGATTTTGACATCTATGGAGAGGACGAAAACCAGGATCCAAGATCCTTCCAGAAGAGAACCAGACACTACTTTATCGCCGCTGTGGAGCAGCTGTGGGACTATGGGATGTCCGAAAGCCCACGGGCCCTGAGGAACAGAGCTCAGAATGGAGAGGTGCCCCGCTTCAAGAAAGTCGTGTTCCGGGAGTTTGCCGACGGCAGCTTTACCCAGCCATCTTACAGGGGGGAGCTGAACAAGCATCTGGGGCTGCTGGGACCCTATATCAGAGCCGAGGTCGAAGATAACATCATGGTGACCTTCAAGAATCAGGCTTCTCGCCCCTACTCCTTTTATTCTTCCCTGATCTCCTACCCTGACGATCAGGAGCAGGGCGCCGAACCTAGGCACAACTTCGTGCAGCCAAATGAGACCAGAACCTACTTTTGGAAGGTGCAGCATCACATGGCTCCCACCGAGGATGAATTCGACTGCAAAGCTTGGGCCTATTTTTCCGATGTCGACCTGGAGAAGGACGTGCATAGCGGCCTGATCGGGCCTCTGCTGATCTGTCGCGCCAACACCCTGAATGCTGCTCACGGAAGACAGGTCACCGTGCAGGAGTTCGCTCTGTTCTTTACCATCTTTGACGAAACCAAGAGCTGGTACTTCACCGAGAACGTGGAAAGGAATTGCAGAGCCCCCTGTCATCTGCAGATGGAGGACCCTACCCTGAAGGAAAACTACAGGTTCCACGCCATCAATGGATATGTCATGGATACCCTGCCCGGCCTGGTCATGGCTCAGAACCAGCGCATCCGGTGGTACCTGCTGTCTATGGGATCCAACGAGAATATCCATAGCATCCACTTCTCTGGCCATGTCTTTTCCGTGAGGAAGAAAGAGGAATACAAAATGGCCGTGTACAATCTGTATCCTGGGGTCTTCGAGACCGTGGAAATGCTGCCAAGCAAAGTGGGAATCTGGAGAATCGAGTGCCTGATCGGCGAACACCTGCAGGCCGGGATGAGCACCACCTTCCTGGTGTACTCTAAGAAATGTCAGACCCCACTGGGGATGGCCTCCGGACATATCCGCGACTTCCAGATCACCGCTAGCGGACAGTACGGACAGTGGGCTCCAAAGCTGGCTAGACTGCACTATTCTGGCTCCATCAACGCCTGGTCTACCAAAGAGCCATTCTCCTGGATCAAGGTGGACCTGCTGGCCCCCATGATCATCCACGGAATCAAAACCCAGGGCGCTAGGCAGAAGTTCAGCTCTCTGTACATCTCCCAGTTTATCATCATGTATAGCCTGGACGGGAAGAAATGGCAGACCTACAGAGGCAATTCCACCGGGACCCTGATGGTCTTCTTTGGAAACGTGGATTCCAGCGGCATCAAGCACAACATCTTCAATCCACCCATCATCGCCCGCTACATCCGGCTGCATCCTACCCACTATAGCATCAGGTCTACCCTGAGAATGGAGCTGATGGGATGCGACCTGAACAGCTGTTCTATGCCACTGGGCATGGAGTCCAAGGCTATCAGCGATGCCCAGATCACCGCTTCTTCCTACTTCACCAATATGTTTGCTACCTGGTCCCCAAGCAAGGCTAGACTGCACCTGCAGGGAAGATCCAACGCTTGGAGACCCCAGGTGAACAATCCTAAGGAGTGGCTGCAGGTCGACTTCCAGAAAACCATGAAGGTCACCGGGGTGACCACCCAGGGAGTGAAATCTCTGCTGACCTCCATGTACGTCAAGGAGTTCCTGATCAGCTCTTCCCAGGACGGCCACCAGTGGACCCTGTTCTTTCAGAACGGCAAGGTCAAAGTGTTCCAGGGGAATCAGGACTCTTTTACCCCCGTCGTGAACTCCCTGGATCCTCCACTGCTGACCAGGTACCTGAGAATCCATCCTCAGAGCTGGGTGCACCAGATCGCTCTGAGAATGGAGGTCCTGGGATGCGAAGCTCAGGACCTGTATTGA

In addition, CpG DNA motifs in the liver-codon optimized coding sequencefor ET3 and HSQ were removed because they may lead to gene methylationand silencing. See Bird, DNA methylation and the frequency of CpG inanimal DNA, 1980, Nucleic Acids Res, 8: 1499-1504. Codons weresubstituted with the most highly used human/liver alternative (based onthe liver-usage bias analysis discussed above) that did not result inthe formation of a 5′-CG-3′ dinucleotide in the sequence. Thesemodifications removed 174 and 175 CpGs from the liver-codon optimizedET3 and HSQ sequences, respectively. CpG removal also helps the vectorevade immune detection, enhancing the safety and efficacy of the vector.See J Clin Invest. 2013, 123(7):2994-3001, entitled “CpG-depletedadeno-associated virus vectors evade immune detection.”

The CpG deleted, liver codon optimized ET3 sequence is SEQ ID NO: 11:ATGCAGCTGGAACTGTCTACCTGTGTGTTTCTGTGTCTGCTGCCTCTGGGGTTTTCTGCTATCAGGAGATACTATCTGGGAGCTGTGGAGCTGTCCTGGGACTACAGGCAGTCTGAGCTGCTGAGAGAACTGCATGTGGATACCAGATTCCCAGCTACAGCTCCAGGAGCTCTGCCTCTGGGCCCATCTGTGCTGTACAAGAAAACAGTCTTTGTGGAGTTTACAGACCAGCTGTTCTCTGTGGCCAGGCCAAGACCACCTTGGATGGGACTGCTGGGACCAACCATCCAGGCTGAGGTGTATGATACAGTGGTGGTGACCCTGAAAAACATGGCCTCCCATCCTGTGAGCCTGCATGCTGTGGGGGTGTCCTTCTGGAAGTCCTCTGAGGGAGCTGAGTATGAAGACCATACCTCCCAGAGGGAGAAAGAAGATGATAAGGTGCTGCCTGGCAAAAGCCAGACCTATGTCTGGCAGGTGCTGAAGGAGAATGGACCAACTGCTTCTGACCCACCATGCCTGACCTACTCTTATCTGTCCCATGTGGATCTGGTGAAGGACCTGAATTCTGGACTGATTGGAGCTCTGCTGGTGTGTAGAGAGGGAAGCCTGACCAGAGAAAGAACCCAGAACCTGCATGAGTTTGTCCTGCTGTTTGCTGTGTTTGATGAAGGGAAGAGCTGGCACTCTGCCAGGAATGACTCCTGGACCAGAGCTATGGATCCAGCTCCTGCTAGAGCTCAGCCTGCTATGCACACAGTCAATGGCTATGTGAATAGGTCTCTGCCAGGACTGATTGGCTGCCATAAGAAATCTGTCTATTGGCATGTGATTGGAATGGGCACCAGCCCTGAGGTGCATTCTATCTTCCTGGAAGGCCACACCTTTCTGGTCAGGCACCATAGACAGGCCTCTCTGGAGATCTCCCCTCTGACCTTCCTGACAGCTCAGACCTTTCTGATGGACCTGGGGCAGTTCCTGCTGTTTTGCCATATCTCTTCCCACCATCATGGAGGAATGGAGGCTCATGTCAGGGTGGAATCCTGTGCTGAGGAACCACAGCTGAGAAGAAAGGCTGATGAGGAAGAGGACTATGATGATAACCTGTATGACTCTGATATGGATGTGGTGAGGCTGGATGGGGATGATGTCAGCCCTTTCATCCAGATCAGGTCTGTGGCCAAGAAACATCCAAAGACCTGGGTCCACTACATTGCTGCTGAAGAGGAAGATTGGGACTATGCCCCCCTGGTGCTGGCTCCTGATGATAGATCCTACAAAAGCCAGTATCTGAACAATGGGCCCCAGAGGATTGGAAGGAAGTACAAGAAAGTGAGGTTCATGGCCTATACAGATGAGACCTTTAAGACCAGAGAGGCTATCCAGCATGAATCTGGGATCCTGGGACCTCTGCTGTATGGAGAAGTGGGGGATACCCTGCTGATCATCTTCAAGAACCAGGCCTCCAGGCCATACAATATCTATCCCCATGGCATCACAGATGTGAGACCACTGTACAGCAGGAGACTGCCCAAGGGGGTCAAACACCTGAAGGATTTCCCCATCCTGCCTGGAGAGATCTTTAAGTATAAATGGACAGTCACAGTGGAAGATGGGCCTACCAAGTCTGATCCAAGGTGCCTGACCAGATACTATAGCTCTTTTGTGAACATGGAGAGAGACCTGGCTTCTGGACTGATTGGACCCCTGCTGATCTGTTACAAAGAGTCTGTGGACCAGAGGGGCAACCAGATCATGTCTGATAAGAGAAATGTCATCCTGTTCTCTGTGTTTGATGAGAACAGGAGCTGGTACCTGACAGAGAACATCCAGAGGTTCCTGCCAAATCCAGCTGGAGTGCAGCTGGAGGACCCAGAATTTCAGGCTTCCAACATCATGCATAGCATCAATGGCTATGTGTTTGATAGCCTGCAGCTGTCTGTCTGCCTGCATGAGGTGGCCTACTGGTATATCCTGTCCATTGGAGCTCAGACAGACTTCCTGTCTGTGTTCTTTAGTGGGTACACCTTTAAGCATAAAATGGTGTATGAGGATACCCTGACCCTGTTCCCCTTTTCTGGGGAGACAGTGTTCATGTCCATGGAAAACCCTGGCCTGTGGATCCTGGGGTGCCACAACTCTGACTTCAGGAATAGAGGAATGACAGCCCTGCTGAAAGTGTCCAGCTGTGATAAGAATACAGGGGATTACTATGAGGACTCTTATGAAGATATCTCTGCTTATCTGCTGAGCAAGAACAATGCCATTGAGCCCAGGTCTTTTGCTCAGAACTCCAGACCTCCATCTGCTTCTGCTCCTAAGCCACCTGTGCTGAGAAGACATCAGAGGGACATCTCCCTGCCTACCTTCCAGCCAGAGGAAGATAAAATGGACTATGATGATATCTTCAGCACAGAGACCAAGGGGGAAGATTTTGACATCTATGGAGAGGATGAAAACCAGGATCCAAGATCCTTCCAGAAGAGAACCAGACACTACTTTATTGCTGCTGTGGAGCAGCTGTGGGACTATGGGATGTCTGAAAGCCCAAGGGCCCTGAGGAACAGAGCTCAGAATGGAGAGGTGCCCAGATTCAAGAAAGTGGTGTTCAGAGAGTTTGCTGATGGCAGCTTTACCCAGCCATCTTACAGGGGGGAGCTGAACAAGCATCTGGGGCTGCTGGGACCCTATATCAGAGCTGAGGTGGAAGATAACATCATGGTGACCTTCAAGAATCAGGCTTCTAGGCCCTACTCCTTTTATTCTTCCCTGATCTCCTACCCTGATGATCAGGAGCAGGGAGCTGAACCTAGGCACAACTTTGTGCAGCCAAATGAGACCAGAACCTACTTTTGGAAGGTGCAGCATCACATGGCTCCCACAGAGGATGAATTTGACTGCAAAGCTTGGGCCTATTTTTCTGATGTGGACCTGGAGAAGGATGTGCATTCTGGCCTGATTGGGCCTCTGCTGATCTGTAGGGCCAACACCCTGAATGCTGCTCATGGAAGACAGGTCACAGTGCAGGAGTTTGCTCTGTTCTTTACCATCTTTGATGAAACCAAGAGCTGGTACTTCACAGAGAATGTGGAAAGGAATTGCAGAGCCCCCTGTCATCTGCAGATGGAGGACCCTACCCTGAAGGAAAACTACAGGTTCCATGCCATCAATGGATATGTCATGGATACCCTGCCTGGCCTGGTCATGGCTCAGAACCAGAGGATCAGATGGTACCTGCTGTCTATGGGATCCAATGAGAATATCCATAGCATCCACTTCTCTGGCCATGTCTTTTCTGTGAGGAAGAAAGAGGAATACAAAATGGCTGTGTACAATCTGTATCCTGGGGTCTTTGAGACAGTGGAAATGCTGCCAAGCAAAGTGGGAATCTGGAGAATTGAGTGCCTGATTGGGGAACACCTGCAGGCTGGGATGAGCACCACCTTCCTGGTGTACTCTAAGAAATGTCAGACCCCACTGGGGATGGCCTCTGGACATATCAGGGACTTCCAGATCACAGCTTCTGGACAGTATGGACAGTGGGCTCCAAAGCTGGCTAGACTGCACTATTCTGGCTCCATCAATGCCTGGTCTACCAAAGAGCCATTCTCCTGGATCAAGGTGGACCTGCTGGCCCCCATGATCATCCATGGAATCAAAACCCAGGGAGCTAGGCAGAAGTTCAGCTCTCTGTACATCTCCCAGTTTATCATCATGTATAGCCTGGATGGGAAGAAATGGCAGACCTACAGAGGCAATTCCACTGGGACCCTGATGGTCTTCTTTGGAAATGTGGATTCCTCTGGCATCAAGCACAACATCTTCAATCCACCCATCATTGCCAGGTACATCAGGCTGCATCCTACCCACTATAGCATCAGGTCTACCCTGAGAATGGAGCTGATGGGATGTGACCTGAACAGCTGTTCTATGCCACTGGGCATGGAGTCCAAGGCTATCTCTGATGCCCAGATCACAGCTTCTTCCTACTTCACCAATATGTTTGCTACCTGGTCCCCAAGCAAGGCTAGACTGCACCTGCAGGGAAGATCCAATGCTTGGAGACCCCAGGTGAACAATCCTAAGGAGTGGCTGCAGGTGGACTTCCAGAAAACCATGAAGGTCACAGGGGTGACCACCCAGGGAGTGAAATCTCTGCTGACCTCCATGTATGTCAAGGAGTTCCTGATCAGCTCTTCCCAGGATGGCCACCAGTGGACCCTGTTCTTTCAGAATGGCAAGGTCAAAGTGTTCCAGGGGAATCAGGACTCTTTTACCCCAGTGGTGAACTCCCTGGATCCTCCACTGCTGACCAGGTACCTGAGAATCCATCCTCAGAGCTGGGTGCACCAGATTGCTCTGAGAATGGAGGTCCTGGGATGTGAAGCTCAGGACCTGTATTGA.The CpG deleted, liver codon optimized HSQ sequence is SEQ ID NO: 2:ATGCAGATTGAACTGTCTACCTGTTTCTTTCTGTGCCTGCTGAGGTTTTGTTTTTCTGCTACCAGAAGATACTACCTGGGAGCTGTGGAACTGAGCTGGGATTACATGCAGTCTGACCTGGGAGAGCTGCCTGTGGATGCTAGATTCCCACCTAGAGTCCCTAAGTCCTTCCCCTTCAACACCTCTGTGGTCTACAAGAAAACCCTGTTTGTGGAGTTTACAGACCACCTGTTCAACATTGCTAAGCCTAGACCACCATGGATGGGACTGCTGGGACCAACCATCCAGGCAGAGGTGTATGACACAGTGGTCATCACCCTGAAAAACATGGCTTCTCACCCTGTGTCCCTGCATGCTGTGGGAGTCTCCTACTGGAAGGCCTCTGAAGGGGCTGAGTATGATGATCAGACCAGCCAGAGGGAAAAAGAGGATGATAAGGTGTTCCCTGGAGGGTCCCATACCTATGTGTGGCAGGTCCTGAAGGAGAATGGACCAATGGCTTCTGACCCTCTGTGCCTGACCTACTCTTATCTGTCCCATGTGGACCTGGTCAAGGATCTGAACTCTGGCCTGATTGGGGCTCTGCTGGTGTGTAGGGAAGGGTCCCTGGCCAAGGAGAAAACCCAGACCCTGCATAAGTTCATCCTGCTGTTTGCTGTGTTTGATGAAGGAAAAAGCTGGCACTCTGAGACCAAGAACTCTCTGATGCAGGACAGGGATGCTGCTTCTGCCAGAGCTTGGCCCAAGATGCACACAGTGAATGGCTATGTCAATAGGAGCCTGCCTGGACTGATTGGCTGCCACAGAAAGTCTGTGTATTGGCATGTCATTGGAATGGGCACCACCCCTGAAGTGCACAGCATCTTCCTGGAGGGGCATACCTTTCTGGTCAGGAACCACAGGCAGGCTAGCCTGGAGATCTCTCCAATCACCTTCCTGACAGCCCAGACCCTGCTGATGGACCTGGGACAGTTCCTGCTGTTTTGCCACATCTCCAGCCACCAGCATGATGGCATGGAGGCTTATGTGAAAGTGGACTCCTGTCCTGAGGAACCTCAGCTGAGGATGAAGAACAATGAGGAAGCTGAAGACTATGATGATGACCTGACAGACTCTGAGATGGATGTGGTCAGGTTTGATGATGATAACTCTCCCTCCTTTATCCAGATCAGGTCTGTGGCCAAGAAACACCCTAAGACCTGGGTCCATTACATTGCTGCTGAGGAAGAGGACTGGGATTATGCTCCACTGGTGCTGGCCCCTGATGATAGATCCTACAAAAGCCAGTATCTGAACAATGGACCCCAGAGGATTGGCAGAAAGTACAAGAAAGTGAGGTTCATGGCTTATACAGATGAGACCTTTAAGACCAGAGAAGCCATCCAGCATGAGTCTGGGATCCTGGGACCTCTGCTGTATGGGGAAGTGGGGGACACCCTGCTGATCATCTTCAAGAACCAGGCCAGCAGGCCTTACAATATCTATCCACATGGCATCACAGATGTGAGACCTCTGTACTCCAGGAGGCTGCCAAAGGGGGTGAAACACCTGAAGGACTTCCCAATCCTGCCTGGGGAAATCTTTAAGTATAAATGGACAGTCACAGTGGAGGATGGGCCCACCAAGTCTGACCCTAGGTGCCTGACCAGATACTATTCTTCCTTTGTGAATATGGAGAGAGACCTGGCTTCTGGACTGATTGGACCCCTGCTGATCTGTTACAAAGAGTCTGTGGATCAGAGGGGCAACCAGATCATGTCTGACAAGAGGAATGTGATCCTGTTCTCTGTCTTTGATGAAAACAGGTCTTGGTACCTGACAGAGAACATCCAGAGGTTCCTGCCTAATCCAGCTGGAGTGCAGCTGGAAGATCCTGAGTTCCAGGCCTCTAACATCATGCATTCCATCAATGGCTATGTGTTTGACTCCCTGCAGCTGTCTGTGTGCCTGCATGAGGTGGCTTACTGGTATATCCTGAGCATTGGAGCCCAGACAGATTTCCTGTCTGTGTTCTTTTCTGGCTACACCTTTAAGCATAAAATGGTGTATGAGGACACCCTGACCCTGTTCCCATTTTCTGGAGAAACTGTGTTCATGAGCATGGAGAATCCTGGGCTGTGGATCCTGGGATGCCACAACTCTGATTTCAGGAATAGAGGGATGACAGCCCTGCTGAAAGTGAGCTCTTGTGACAAGAACACAGGAGACTACTATGAAGATAGCTATGAGGACATCTCTGCTTATCTGCTGTCCAAAAACAATGCCATTGAGCCCAGGAGCTTCTCTCAGAACCCTCCAGTGCTGAAGAGGCACCAGAGGGAGATCACCAGAACCACCCTGCAGTCTGATCAGGAAGAGATTGACTATGATGATACCATCTCTGTGGAAATGAAGAAAGAGGACTTTGATATCTATGATGAAGATGAGAACCAGTCTCCCAGGTCCTTCCAGAAGAAAACCAGACATTACTTTATTGCTGCTGTGGAGAGGCTGTGGGACTATGGCATGTCCAGCTCTCCTCATGTGCTGAGAAATAGAGCTCAGTCTGGATCTGTCCCACAGTTCAAGAAAGTGGTCTTCCAGGAGTTTACAGATGGAAGCTTTACCCAGCCACTGTACAGGGGAGAACTGAATGAGCACCTGGGGCTGCTGGGACCCTATATCAGGGCTGAAGTGGAGGATAACATCATGGTCACCTTCAGGAATCAGGCCAGCAGACCCTACTCTTTTTATTCCAGCCTGATCTCCTATGAAGAGGACCAGAGACAGGGAGCTGAACCAAGAAAAAACTTTGTGAAGCCTAATGAGACCAAAACCTACTTTTGGAAGGTGCAGCACCATATGGCCCCTACCAAAGATGAGTTTGATTGCAAGGCCTGGGCTTATTTTTCTGATGTGGATCTGGAGAAGGATGTCCACTCTGGCCTGATTGGGCCACTGCTGGTGTGTCATACCAACACCCTGAATCCAGCTCATGGAAGGCAGGTGACAGTCCAGGAATTTGCCCTGTTCTTTACCATCTTTGATGAGACCAAGAGCTGGTACTTCACAGAAAACATGGAGAGGAATTGCAGAGCCCCATGTAACATCCAGATGGAAGACCCCACCTTCAAGGAGAACTACAGATTTCATGCTATCAATGGGTATATCATGGATACCCTGCCAGGACTGGTCATGGCTCAGGACCAGAGGATCAGATGGTACCTGCTGAGCATGGGGTCTAATGAGAATATCCACTCCATCCATTTCTCTGGACATGTGTTTACAGTAAGGAAGAAAGAAGAGTACAAGATGGCCCTGTACAACCTGTATCCTGGGGTGTTTGAAACAGTGGAGATGCTGCCTTCCAAGGCTGGGATCTGGAGGGTGGAATGCCTGATTGGGGAGCACCTGCATGCTGGAATGTCTACCCTGTTCCTGGTGTACTCCAATAAGTGTCAGACCCCCCTGGGGATGGCTTCTGGACATATCAGGGACTTCCAGATCACAGCTTCTGGACAGTATGGACAGTGGGCTCCTAAGCTGGCTAGACTGCACTATTCTGGCTCCATCAATGCTTGGTCTACCAAAGAGCCTTTCTCCTGGATCAAGGTGGACCTGCTGGCTCCAATGATCATCCATGGCATCAAAACCCAGGGGGCCAGGCAGAAGTTCTCTTCCCTGTACATCAGCCAGTTTATCATCATGTATTCTCTGGATGGGAAGAAATGGCAGACCTACAGAGGCAATTCCACAGGGACCCTGATGGTGTTCTTTGGCAATGTGGACAGCTCTGGGATCAAGCACAACATCTTCAATCCCCCTATCATTGCCAGGTACATCAGACTGCACCCAACCCATTATTCCATCAGGAGCACCCTGAGAATGGAGCTGATGGGGTGTGATCTGAACAGCTGTTCTATGCCCCTGGGAATGGAGTCTAAGGCCATCTCTGATGCTCAGATCACAGCCTCCAGCTACTTCACCAATATGTTTGCTACCTGGTCCCCAAGCAAGGCTAGACTGCATCTGCAGGGAAGAAGCAATGCTTGGAGACCACAGGTGAACAATCCCAAGGAGTGGCTGCAGGTGGACTTCCAGAAAACCATGAAGGTGACAGGAGTCACCACCCAGGGAGTGAAAAGCCTGCTGACCTCTATGTATGTCAAGGAGTTCCTGATCTCTTCCAGCCAGGATGGGCACCAGTGGACCCTGTTCTTTCAGAATGGAAAGGTGAAAGTCTTCCAGGGCAATCAGGATTCCTTTACCCCTGTGGTCAACAGCCTGGACCCACCCCTGCTGACCAGGTACCTGAGAATCCACCCACAGTCCTGGGTGCATCAGATTGCTCTGAGGATGGAAGTCCTGGGCTGTGAGGCCCAGGACCTGTATTGA

This approach increased the LCAI from 0.62 to 0.86 for B domain deletedhuman fVIII (HSQ). In vitro expression of the optimized fVIII sequenceswas assessed in HepG2 cells transiently transfected with correspondingfVIII expression plasmids. The codon-optimization in the nucleic acidsequence coding for HSQ increased expression of HSQ 7.4 fold, andexpressed as efficiently as non-codon optimized ET3 (FIG. 3A). Thecodon-optimization in the nucleic acid sequence coding for HSQ increasedexpression of ET3 5.6 fold. When tested in vivo by hydrodynamicinjection of plasmid carrying the codon optimized fVIII variants intomice, HSQ activity rose to levels that could be detected by the assaywhich were nearly equivalent to the fVIII levels seen in the non-codonoptimized ET3 (FIG. 3B). Further, a 17 fold increase in activity wasobserved for the codon optimized ET3 (FIG. 3B).

Translation efficacy can sometimes also be improved through optimizationof GC content, mRNA secondary structure, premature PolyA sites, RNAinstability motif, stable free energy of mRNA, internal chi sites,ribosomal binding sites, cryptic splicing sites, negative CpG islands,SD sequence, TATA boxes, and cyptic terminal signals, etc. FIG. 4illustrates changes that were made to an AAV cassette encoding the ET3codon-optimized CpG deleted sequence to increase its production. Severalcis-acting elements within the HSQ sequence were additional modified toincrease fVIII expression, as summarized in the following table.

CIS-Acting Elements Optimized Original Splice(GGTAAG) 0 2 Splice(GGTGAT}0 1 PolyA(AATAAA)(4789 - 1 1 AATAAA) PolyA(ATTAAA) 0 0Destabilizing{ATTTA) 0 6 PolyT(TTTTTT)(4827 - 1 2 TTTTTT) PolyA(AAAAAAA)0 1

In addition to the liver-optimized codon sequences provided above, theencoding sequence for the ET3 and HSQ fVIII proteins werecodon-optimized for expression in myeloid cells. Using the sequences ofhighly expressed genes in the human myeloid cells, a custom codon-usagebias table specific for the human liver was constructed (see FIG. 2C)that differs substantially from the most prevalent codons used in totalhuman coding sequences (FIG. 2B). Optimized coding sequence of the ET3and HSQ variants of fVIII was developed with the most statisticallyprevalent codons identified by the liver-usage bias analysis. Inaddition, CpG DNA motifs in the myeloid-codon optimized coding sequencefor ET3 and HSQ were removed because they may lead to gene methylationand silencing.

The CpG deleted, myeloid codon optimized ET3 sequence is SEQ ID NO: 125:ATGCAGCTGGAGCTCTCAACCTGTGTGTTCCTCTGCCTGCTCCCCCTGGGATTTTCAGCTATCAGGAGATACTATCTGGGAGCAGTGGAACTGTCCTGGGACTACAGGCAGTCAGAGCTGCTCAGAGAACTGCATGTGGATACTAGGTTCCCTGCAACAGCTCCTGGAGCACTGCCACTGGGACCTTCAGTGCTGTACAAGAAAACTGTCTTTGTGGAGTTTACAGACCAGCTGTTCAGTGTGGCCAGGCCCAGGCCCCCCTGGATGGGGCTGCTGGGACCCACCATCCAGGCTGAAGTGTATGATACTGTGGTGGTGACCCTGAAAAACATGGCCTCTCATCCAGTCAGCCTGCATGCTGTGGGAGTGAGCTTCTGGAAGAGCAGTGAGGGAGCTGAGTATGAAGACCATACCTCACAGAGGGAGAAAGAAGATGATAAGGTGCTGCCAGGAAAAAGCCAGACCTATGTGTGGCAGGTGCTGAAGGAGAATGGCCCTACAGCTTCAGATCCTCCCTGCCTCACATACTCTTATCTGAGCCATGTGGATCTGGTGAAGGACCTCAATAGTGGCCTGATTGGGGCACTGCTGGTGTGCAGAGAGGGGTCCCTCACAAGGGAAAGAACTCAGAACCTGCATGAGTTTGTCCTGCTCTTTGCTGTGTTTGATGAGGGAAAGTCCTGGCACTCAGCAAGGAATGACAGCTGGACCAGGGCTATGGACCCAGCACCAGCCAGAGCTCAGCCAGCTATGCACACTGTCAATGGCTATGTGAATAGGTCCCTGCCTGGACTCATTGGCTGCCATAAGAAATCAGTCTATTGGCATGTGATTGGAATGGGCACCAGCCCAGAGGTGCATTCCATCTTCCTGGAAGGCCACACATTTCTGGTCAGGCACCATAGACAGGCCAGCCTGGAGATCAGCCCACTGACTTTCCTCACAGCACAGACATTTCTGATGGACCTGGGGCAGTTCCTGCTCTTTTGCCATATCTCAAGTCACCATCATGGAGGGATGGAGGCTCATGTCAGGGTGGAAAGCTGTGCAGAGGAACCTCAGCTGAGGAGGAAGGCAGATGAGGAAGAGGACTATGATGATAACCTGTATGACTCAGATATGGATGTGGTGAGGCTGGATGGAGATGATGTCAGCCCATTCATCCAGATCAGGTCAGTGGCTAAGAAACACCCTAAGACCTGGGTCCACTACATTGCAGCTGAAGAGGAAGATTGGGACTATGCACCCCTGGTGCTGGCCCCAGATGATAGAAGTTACAAATCTCAGTATCTGAACAATGGGCCCCAGAGGATTGGAAGGAAGTACAAGAAAGTGAGGTTCATGGCTTATACTGATGAGACCTTTAAGACAAGAGAGGCAATCCAGCATGAAAGTGGCATCCTGGGACCACTGCTCTATGGAGAAGTGGGGGATACCCTGCTCATCATCTTCAAGAACCAGGCCTCAAGGCCTTACAATATCTATCCCCATGGCATCACAGATGTGAGGCCTCTCTACAGCAGGAGACTGCCCAAGGGAGTCAAACACCTCAAGGATTTCCCCATCCTGCCAGGGGAAATCTTCAAGTATAAATGGACAGTCACTGTGGAAGATGGGCCAACTAAGTCAGATCCTAGGTGCCTGACCAGGTACTATTCTAGCTTTGTGAACATGGAGAGGGACCTGGCTTCAGGACTGATTGGACCTCTGCTCATCTGCTACAAAGAATCAGTGGACCAGAGGGGCAACCAGATCATGAGTGATAAGAGAAATGTCATCCTGTTCTCAGTGTTTGATGAGAATAGGAGTTGGTATCTGACAGAAAACATCCAGAGGTTCCTGCCTAATCCTGCAGGAGTGCAGCTGGAGGACCCAGAATTTCAGGCTTCAAACATCATGCATAGTATCAATGGCTATGTGTTTGATAGTCTGCAGCTCTCTGTCTGCCTGCATGAGGTGGCCTACTGGTATATCCTCAGCATTGGAGCTCAGACTGACTTCCTGAGTGTGTTCTTTTCAGGCTACACATTCAAGCATAAGATGGTCTATGAAGATACCCTGACACTCTTCCCCTTTTCTGGGGAGACTGTGTTTATGAGCATGGAAAACCCAGGCCTGTGGATTCTGGGGTGCCACAACAGTGACTTCAGGAATAGAGGGATGACTGCTCTGCTCAAAGTGTCCTCATGTGATAAGAATACTGGAGATTACTATGAGGACTCTTATGAAGATATCAGTGCATATCTGCTCTCCAAAAACAATGCCATTGAGCCCAGGTCATTTGCTCAGAACAGTAGACCACCTTCTGCAAGTGCACCAAAGCCTCCAGTGCTGAGGAGACACCAGAGGGACATCAGCCTGCCAACCTTCCAGCCTGAGGAAGATAAAATGGACTATGATGATATCTTCTCCACTGAGACCAAGGGGGAAGATTTTGACATCTATGGAGAGGATGAAAACCAGGACCCCAGGTCCTTCCAGAAGAGGACCAGACACTACTTTATTGCAGCTGTGGAGCAGCTGTGGGACTATGGCATGTCTGAATCACCTAGAGCTCTGAGGAACAGAGCACAGAATGGGGAGGTGCCCAGGTTCAAGAAAGTGGTGTTCAGAGAATTTGCAGATGGCTCTTTTACCCAGCCTAGCTACAGGGGGGAGCTCAACAAGCATCTGGGGCTGCTGGGACCCTATATCAGAGCAGAGGTGGAAGATAACATCATGGTGACATTCAAGAATCAGGCCTCAAGACCCTACAGTTTTTATAGTTCTCTGATCAGCTACCCAGATGATCAGGAGCAGGGGGCTGAACCAAGGCACAACTTTGTGCAGCCTAATGAGACAAGAACTTACTTTTGGAAGGTCCAGCATCACATGGCTCCCACAGAGGATGAGTTTGACTGCAAGGCCTGGGCATATTTTTCTGATGTGGACCTGGAGAAGGATGTGCATAGTGGCCTCATTGGGCCACTGCTCATCTGCAGGGCAAACACACTGAATGCTGCACATGGCAGGCAGGTCACTGTGCAGGAGTTTGCCCTGTTCTTTACAATCTTTGATGAAACTAAGTCCTGGTACTTCACAGAGAATGTGGAAAGGAATTGCAGAGCCCCCTGCCATCTCCAGATGGAGGACCCAACTCTGAAGGAAAACTACAGGTTCCATGCTATCAATGGATATGTCATGGATACACTGCCAGGCCTGGTGATGGCACAGAACCAGAGGATCAGGTGGTATCTGCTCAGCATGGGGTCCAATGAGAATATCCATTCTATCCACTTCTCAGGACATGTCTTTTCAGTGAGGAAGAAAGAGGAATATAAAATGGCTGTGTACAATCTGTATCCAGGGGTCTTTGAGACAGTGGAAATGCTGCCTAGCAAAGTGGGGATCTGGAGAATTGAGTGCCTCATTGGAGAACACCTGCAGGCAGGGATGTCCACCACATTTCTGGTGTACTCAAAGAAATGCCAGACTCCCCTGGGGATGGCAAGTGGACATATCAGGGACTTCCAGATCACTGCATCAGGACAGTATGGACAGTGGGCACCAAAGCTGGCTAGGCTCCACTATAGTGGCTCTATCAATGCTTGGAGTACCAAAGAGCCTTTCTCTTGGATCAAGGTGGATCTGCTGGCCCCCATGATCATCCATGGAATCAAAACACAGGGAGCTAGACAGAAGTTCAGCTCCCTGTACATCAGTCAGTTTATCATCATGTATTCTCTGGATGGGAAGAAATGGCAGACCTACAGGGGCAATAGCACTGGGACACTGATGGTCTTCTTTGGAAATGTGGATTCAAGTGGCATCAAGCACAACATCTTCAATCCTCCCATCATTGCCAGGTACATCAGACTGCATCCCACACACTATTCAATCAGGAGTACTCTCAGAATGGAGCTGATGGGGTGTGACCTCAACAGCTGCTCCATGCCACTGGGAATGGAATCCAAGGCAATCTCAGATGCCCAGATCACTGCTTCTAGCTACTTCACCAATATGTTTGCAACATGGTCACCCAGTAAAGCAAGGCTGCACCTCCAGGGAAGGTCCAATGCTTGGAGACCCCAGGTGAACAATCCAAAGGAGTGGCTGCAGGTGGACTTTCAGAAAACCATGAAGGTCACAGGGGTGACTACCCAGGGAGTGAAAAGTCTGCTCACCTCTATGTATGTCAAGGAGTTCCTGATCTCCTCAAGTCAGGATGGCCACCAGTGGACACTGTTCTTTCAGAATGGCAAGGTCAAAGTGTTCCAGGGGAATCAGGACAGCTTTACACCAGTGGTGAACAGCCTGGACCCCCCTCTGCTCACTAGATATCTGAGAATCCATCCACAGAGCTGGGTGCACCAGATTGCACTCAGAATGGAGGTCCTGGGCTGTGAAGCCCAGGACCTGTATTGAThe CpG deleted, myeloid codon optimized HSQ sequence is SEQ ID NO: 126:ATGCAGATTGAGCTCAGCACCTGCTTCTTTCTGTGCCTGCTCAGGTTCTGCTTTTCAGCCACAAGGAGATACTATCTGGGAGCTGTGGAACTGTCATGGGATTACATGCAGAGTGACCTGGGAGAGCTCCCTGTGGATGCTAGGTTCCCCCCAAGGGTCCCAAAGTCTTTCCCTTTTAATACCAGTGTGGTCTATAAGAAAACACTCTTTGTGGAATTTACTGATCACCTGTTCAACATTGCAAAGCCAAGGCCTCCCTGGATGGGACTGCTGGGACCTACCATCCAGGCTGAGGTGTATGACACTGTGGTCATCACACTGAAAAACATGGCATCTCACCCTGTCAGCCTGCATGCAGTGGGAGTCAGCTACTGGAAGGCTTCAGAAGGGGCAGAGTATGATGATCAGACAAGCCAGAGAGAAAAAGAGGATGATAAGGTGTTCCCAGGAGGGAGCCATACTTATGTGTGGCAGGTCCTGAAGGAGAATGGCCCAATGGCCAGTGACCCACTGTGCCTCACCTACTCATATCTGAGTCATGTGGACCTGGTCAAGGATCTCAACTCAGGCCTGATTGGGGCACTGCTGGTGTGCAGGGAAGGCTCACTGGCCAAGGAGAAAACCCAGACACTGCATAAGTTCATCCTGCTCTTTGCTGTGTTTGATGAAGGGAAATCTTGGCACAGTGAGACCAAGAACAGTCTGATGCAGGACAGGGATGCTGCTTCTGCCAGAGCTTGGCCCAAGATGCACACAGTGAATGGATATGTCAATAGGTCCCTGCCAGGACTCATTGGCTGCCACAGAAAGTCAGTGTATTGGCATGTCATTGGAATGGGCACCACACCAGAAGTGCACAGCATCTTCCTGGAGGGGCATACCTTTCTGGTCAGGAACCACAGGCAGGCCAGCCTGGAGATCAGCCCAATCACCTTCCTGACAGCCCAGACTCTGCTCATGGATCTGGGGCAGTTCCTGCTCTTTTGCCACATCAGCTCCCACCAGCATGATGGAATGGAGGCATATGTGAAAGTGGACTCCTGCCCAGAGGAACCACAGCTGAGGATGAAGAACAATGAGGAAGCTGAAGACTATGATGATGACCTGACAGACTCAGAGATGGATGTGGTCAGGTTTGATGATGATAACAGCCCCTCCTTTATCCAGATCAGAAGTGTGGCCAAGAAACACCCAAAGACATGGGTCCATTACATTGCAGCTGAGGAAGAGGACTGGGATTATGCACCTCTGGTGCTGGCCCCAGATGATAGATCCTACAAATCACAGTATCTGAACAATGGACCCCAGAGGATTGGCAGAAAGTACAAGAAAGTGAGGTTCATGGCCTATACTGATGAAACATTTAAGACTAGAGAAGCTATCCAGCATGAGTCAGGCATCCTGGGACCACTGCTCTATGGAGAAGTGGGGGACACCCTGCTCATCATCTTCAAGAACCAGGCTTCCAGGCCATACAATATCTATCCTCATGGCATCACAGATGTGAGACCACTCTACTCAAGGAGACTGCCTAAGGGAGTCAAACACCTCAAGGACTTCCCTATCCTGCCAGGGGAAATCTTTAAGTATAAATGGACTGTGACAGTGGAGGATGGGCCCACTAAGAGTGACCCAAGGTGCCTGACCAGATACTATTCAAGTTTTGTGAATATGGAAAGGGATCTGGCATCAGGACTGATTGGACCTCTGCTCATCTGCTACAAAGAGAGTGTGGATCAGAGGGGCAACCAGATCATGTCAGACAAGAGGAATGTGATCCTGTTCAGTGTCTTTGATGAAAACAGGTCTTGGTATCTGACAGAGAACATCCAGAGATTCCTGCCAAATCCTGCAGGGGTGCAGCTGGAAGATCCAGAGTTTCAGGCCTCAAACATCATGCATAGTATCAATGGATATGTGTTTGACAGTCTGCAGCTCTCTGTGTGCCTGCATGAAGTGGCCTACTGGTATATCCTGTCCATTGGAGCTCAGACAGATTTCCTGAGTGTGTTCTTTTCAGGCTACACTTTTAAGCATAAAATGGTCTATGAGGACACACTGACTCTCTTCCCTTTTAGTGGGGAAACAGTGTTTATGAGCATGGAGAATCCAGGGCTGTGGATTCTGGGATGCCACAACAGTGATTTCAGGAATAGAGGCATGACTGCTCTGCTCAAAGTGTCTAGCTGTGACAAGAACACAGGGGACTACTATGAAGATTCTTATGAGGACATCAGTGCTTATCTGCTCTCCAAAAACAATGCAATTGAACCCAGATCATTCAGTCAGAATCCACCTGTGCTGAAGAGGCACCAGAGAGAGATCACTAGGACTACCCTGCAGTCAGATCAGGAAGAGATTGACTATGATGATACCATCTCAGTGGAAATGAAGAAAGAGGACTTTGATATCTATGATGAAGATGAGAACCAGAGTCCAAGGTCTTTCCAGAAGAAAACCAGACATTACTTTATTGCTGCAGTGGAGAGGCTGTGGGATTATGGAATGTCCTCAAGTCCACATGTGCTGAGGAATAGGGCACAGTCTGGCAGTGTCCCTCAGTTCAAGAAAGTGGTCTTCCAGGAGTTTACAGATGGCAGCTTCACTCAGCCTCTGTACAGGGGAGAACTCAATGAGCACCTGGGGCTGCTGGGACCCTATATCAGAGCTGAAGTGGAGGATAACATCATGGTCACCTTCAGGAATCAGGCTTCAAGACCCTACAGTTTTTATTCTAGCCTGATCAGCTATGAAGAGGACCAGAGGCAGGGAGCTGAACCTAGGAAAAACTTTGTGAAGCCAAATGAGACCAAAACATACTTTTGGAAGGTCCAGCACCACATGGCACCAACCAAAGATGAGTTTGATTGCAAGGCATGGGCCTATTTTTCAGATGTGGATCTGGAGAAGGATGTCCACAGTGGCCTCATTGGGCCTCTGCTGGTGTGCCATACTAACACCCTGAATCCAGCTCATGGCAGGCAGGTGACAGTCCAGGAGTTTGCACTGTTCTTTACCATCTTTGATGAGACAAAGTCCTGGTACTTCACTGAAAACATGGAGAGGAATTGCAGAGCTCCTTGCAACATCCAGATGGAAGACCCCACCTTCAAGGAGAACTACAGATTTCATGCAATCAATGGGTATATCATGGATACACTGCCAGGACTGGTGATGGCCCAGGACCAGAGGATCAGATGGTATCTGCTCAGCATGGGGTCCAATGAGAATATCCACTCTATCCATTTCAGTGGACATGTGTTTACAGTCAGAAAGAAAGAAGAGTATAAAATGGCCCTGTACAACCTCTATCCAGGAGTGTTTGAAACAGTGGAGATGCTGCCAAGCAAGGCTGGGATCTGGAGGGTGGAATGCCTCATTGGGGAGCACCTGCATGCAGGAATGTCAACCCTGTTTCTGGTCTACAGTAATAAGTGCCAGACACCTCTGGGAATGGCAAGTGGACATATCAGGGATTTCCAGATCACTGCTAGTGGACAGTATGGACAGTGGGCACCAAAGCTGGCTAGACTCCACTATTCAGGCTCAATCAATGCTTGGTCCACCAAAGAGCCATTCTCATGGATCAAGGTGGACCTGCTGGCTCCTATGATCATCCATGGCATCAAAACACAGGGGGCAAGGCAGAAGTTCTCCTCACTGTACATCTCTCAGTTTATCATCATGTATAGCCTGGATGGCAAGAAATGGCAGACCTACAGGGGCAATAGCACAGGGACTCTGATGGTGTTCTTTGGCAATGTGGACAGCAGTGGGATCAAGCACAACATCTTCAATCCCCCAATCATTGCAAGGTACATCAGACTGCACCCCACCCATTATTCAATCAGGAGTACACTCAGGATGGAACTGATGGGGTGTGATCTCAACAGTTGCTCTATGCCACTGGGAATGGAGTCCAAGGCAATCTCAGATGCCCAGATCACTGCTAGCTCCTACTTCACTAATATGTTTGCTACCTGGAGCCCCTCCAAAGCAAGGCTGCACCTCCAGGGAAGGAGCAATGCATGGAGGCCTCAGGTGAACAATCCCAAGGAATGGCTGCAGGTGGATTTCCAGAAAACTATGAAGGTGACTGGAGTCACAACTCAGGGAGTGAAAAGTCTGCTCACTTCTATGTATGTCAAGGAGTTCCTGATCTCAAGTTCTCAGGATGGCCACCAGTGGACCCTGTTCTTTCAGAATGGAAAGGTGAAAGTCTTCCAGGGCAATCAGGATTCCTTTACACCAGTGGTCAACTCACTGGACCCTCCCCTGCTCACTAGATATCTGAGAATCCACCCTCAGAGCTGGGTGCATCAGATTGCTCTCAGAATGGAAGTCCTGGGCTGTGAGGCACAGGACCTGTATTGA

In vitro expression of the non-optimized, liver-optimized, and myeloidoptimized fVIII sequences was assessed in HepG2 cells transientlytransfected with corresponding fVIII expression plasmids (FIG. 5). Thetissue specific optimization lead to increased FVIII activity in theHepG2 (hepatic) cells expressing the liver-optimized fVIII compared toeither non-optimized or myeloid optimized forms of ET3 or HSQ. Theseresults show that liver optimization specifically benefits expression inhepatocyte derived cells and that expression of myeloid-optimized FVIIIdoes not benefit expression in HepG2 cells.

Further, when these experiments were repeated using non-human cells(baby hamster kidney cells), it was found that the human-specificsequence optimization led to decreased expression in the non-human cells(FIG. 6).

Factor IX

Similar to the codon-optimization for clotting fVIII discussed above,fIX sequences were also codon optimized for expression in hepatocytesusing the same codon optimization tables used for clotting factor fVIII.The fIX sequences selected for optimization include fIX with thepro-thrombogenic “Padua” mutation R338L (“fIX Padua,” see Paolo et al,“X-Linked Thrombophilia with a Mutant Factor IX” N Engl J Med;361:1671-1675, 2009) and fIX with the thrombophelic “Malmo” variant 148T(fIX Malmo,” see Graham et al, “The Malmo Polymorphism of CoagulationFactor IX, An Immunologic Polymorphism Due to Dimorphism of Residue 148That Is in Linkage Disequilibrium with Two Other FIX Polymorphisms,” Am.J. Hum. Genet. 42:573-580, 1988)

Liver and myeloid optimized fIX cDNAs were designed and optimizedaccording to the liver and myeloid tables shown in FIG. 2. All instancesof “cg” in their sequence removed through synonymous codon substitution.Both cDNAs incorporate the Padua and Malmo substitutions.

Liver codon optimized fIX with Padua/Malmomutations and no CpG (Version 1) (SEQ ID NO: 124)ATGCAGAGGGTCAATATGATCATGGCTGAATCTCCTGGGCTGATCACCATTTGCCTGCTGGGATACCTGCTGTCTGCTGAGTGTACAGTGTTCCTGGACCATGAGAATGCCAATAAGATCCTGAACAGGCCCAAAAGATACAATTCTGGAAAGCTGGAGGAATTTGTGCAGGGCAACCTGGAGAGGGAATGCATGGAGGAAAAGTGTAGCTTTGAGGAAGCTAGGGAGGTGTTTGAAAACACAGAGAGGACCACAGAATTCTGGAAGCAGTATGTGGATGGAGATCAGTGTGAGTCCAACCCCTGTCTGAATGGAGGGTCTTGCAAAGATGATATCAACTCCTATGAGTGCTGGTGTCCTTTTGGATTTGAAGGCAAAAATTGTGAGCTGGATGTGACCTGTAACATCAAGAATGGCAGGTGTGAGCAGTTCTGTAAAAACTCTGCTGATAATAAGGTGGTCTGCAGCTGTACAGAAGGCTATAGGCTGGCTGAGAACCAGAAGAGCTGTGAACCAGCTGTGCCCTTCCCTTGTGGGAGGGTGTCTGTCAGCCAGACCTCTAAGCTGACCAGAGCTGAGACTGTGTTCCCAGATGTGGATTATGTCAACTCCACAGAGGCTGAAACCATCCTGGACAACATCACCCAGTCTACCCAGTCCTTCAATGACTTTACCAGAGTGGTGGGAGGAGAGGATGCCAAACCAGGCCAGTTCCCCTGGCAGGTGGTCCTGAATGGGAAGGTGGATGCTTTTTGTGGGGGATCCATTGTGAATGAGAAATGGATTGTCACAGCTGCTCACTGTGTGGAGACAGGGGTCAAGATCACTGTGGTGGCTGGAGAGCACAACATTGAGGAAACAGAACATACTGAGCAGAAGAGGAATGTGATCAGAATCATCCCTCACCATAACTACAATGCTGCTATCAACAAATATAATCATGACATTGCCCTGCTGGAACTGGATGAGCCTCTGGTGCTGAACAGCTATGTCACCCCAATCTGCATTGCTGACAAAGAGTATACCAATATCTTCCTGAAGTTTGGATCTGGATATGTGTCTGGATGGGGAAGGGTCTTCCACAAGGGCAGGTCTGCCCTGGTGCTGCAGTATCTGAGGGTGCCTCTGGTGGACAGAGCTACCTGCCTGCTGTCTACCAAGTTCACCATCTACAACAATATGTTCTGTGCTGGATTTCATGAGGGAGGCAGGGACTCCTGTCAGGGGGATTCTGGAGGCCCACATGTGACAGAGGTGGAAGGCACCAGCTTCCTGACTGGCATCATCTCTTGGGGGGAGGAATGTGCTATGAAGGGGAAATATGGAATCTACACCAAAGTGAGCAGGTATGTGAACTGGATCAAAGAGAAGACCAAACTGACCTGALiver-Codon Optimized fIX with no CpG encoding A582 modifications(SEQ ID NO: 8) ATGCAGAGGGTGAACATGATCATGGCTGAGTCTCCTGGACTGATCACCATCTGCCTGCTGGGCTATCTGCTGTCTGCTGAGTGTACAGTGTTCCTGGACCATGAAAATGCTAATAAAATCCTGAACAGGCCAAAGAGGTACAATTCTGGGAAACTGGAGGAATTTGTGCAGGGAAACCTGGAGAGGGAATGCATGGAGGAAAAGTGTAGCTTTGAGGAAGCCAGGGAGGTGTTTGAAAATACAGAGAGGACCACAGAGTTCTGGAAACAGTATGTGGATGGGGATCAGTGTGAGTCCAACCCCTGTCTGAATGGAGGGTCTTGCAAGGATGATATCAACTCCTATGAGTGCTGGTGTCCTTTTGGATTTGAAGGCAAGAATTGTGAGCTGGATGTGACCTGTAACATCAAAAATGGGAGGTGTGAGCAGTTCTGTAAGAACTCTGCTGATAATAAAGTGGTCTGCAGCTGTACAGAAGGCTACAGGCTGGCTGAGAACCAGAAGAGCTGTGAACCAGCTGTGCCCTTCCCTTGTGGGAGGGTGTCTGTCAGCCAGACCAGCAAGCTGACCAGAGCTGAGGCTGTGTTTCCTGATGTGGATTATGTCAACTCTACAGAGGCTGAAACCATCCTGGACAACATCACCCAGTCTACCCAGTCCTTCAATGACTTTACCAGGGTGGTGGGAGGGGAGGATGCTAAGCCAGGACAGTTCCCCTGGCAGGTGGTCCTGAATGGCAAAGTGGATGCTTTTTGTGGGGGCTCCATTGTGAATGAGAAGTGGATTGTCACAGCTGCTCACTGTGTGGAAACTGGGGTCAAGATCACAGTGGTGGCTGGAGAGCACAACATTGAGGAAACTGAACATACAGAGCAGAAAAGGAATGTGATCAGAATCATCCCCCACCATAACTACAATGCTGCTATCAACAAGTATAATCATGACATTGCCCTGCTGGAACTGGATGAGCCTCTGGTGCTGAACAGCTATGTCACCCCAATCTGCATTGCTGACAAGGAGTATACCAATATCTTCCTGAAATTTGGGTCTGGATATGTGTCTGGGTGGGGAAGGGTCTTCCACAAGGGAAGGTCTGCTCTGGTGCTGCAGTATCTGAGGGTGCCCCTGGTGGACAGAGCTACCTGCCTGAGGAGCACCAAGTTCACCATCTACAACAATATGTTCTGTGCTGGATTTCATGAGGGAGGGAGGGACTCCTGTCAGGGAGATTCTGGAGGCCCTCATGTGACAGAGGTGGAAGGCACCAGCTTCCTGACTGGCATCATCTCTTGGGGGGAGGAATGTGCTATGAAGGGGAAATATGGAATCTATACCAAGGTGTCCAGATATGTCAACTGGATCAAGGAGAAAACCAAGCTGACCTGALiver codon optimized fIX with no CpGincluding Padua and A582 modifications (SEQ ID NO: 9)ATGCAGAGGGTGAACATGATCATGGCTGAGTCTCCTGGACTGATCACCATCTGCCTGCTGGGCTATCTGCTGTCTGCTGAGTGTACAGTGTTCCTGGACCATGAAAATGCTAATAAAATCCTGAACAGGCCAAAGAGGTACAATTCTGGGAAACTGGAGGAATTTGTGCAGGGAAACCTGGAGAGGGAATGCATGGAGGAAAAGTGTAGCTTTGAGGAAGCCAGGGAGGTGTTTGAAAATACAGAGAGGACCACAGAGTTCTGGAAACAGTATGTGGATGGGGATCAGTGTGAGTCCAACCCCTGTCTGAATGGAGGGTCTTGCAAGGATGATATCAACTCCTATGAGTGCTGGTGTCCTTTTGGATTTGAAGGCAAGAATTGTGAGCTGGATGTGACCTGTAACATCAAAAATGGGAGGTGTGAGCAGTTCTGTAAGAACTCTGCTGATAATAAAGTGGTCTGCAGCTGTACAGAAGGCTACAGGCTGGCTGAGAACCAGAAGAGCTGTGAACCAGCTGTGCCCTTCCCTTGTGGGAGGGTGTCTGTCAGCCAGACCAGCAAGCTGACCAGAGCTGAGGCTGTGTTTCCTGATGTGGATTATGTCAACTCTACAGAGGCTGAAACCATCCTGGACAACATCACCCAGTCTACCCAGTCCTTCAATGACTTTACCAGGGTGGTGGGAGGGGAGGATGCTAAGCCAGGACAGTTCCCCTGGCAGGTGGTCCTGAATGGCAAAGTGGATGCTTTTTGTGGGGGCTCCATTGTGAATGAGAAGTGGATTGTCACAGCTGCTCACTGTGTGGAAACTGGGGTCAAGATCACAGTGGTGGCTGGAGAGCACAACATTGAGGAAACTGAACATACAGAGCAGAAAAGGAATGTGATCAGAATCATCCCCCACCATAACTACAATGCTGCTATCAACAAGTATAATCATGACATTGCCCTGCTGGAACTGGATGAGCCTCTGGTGCTGAACAGCTATGTCACCCCAATCTGCATTGCTGACAAGGAGTATACCAATATCTTCCTGAAATTTGGGTCTGGATATGTGTCTGGGTGGGGAAGGGTCTTCCACAAGGGAAGGTCTGCTCTGGTGCTGCAGTATCTGAGGGTGCCCCTGGTGGACAGAGCTACCTGCCTGCTGAGCACCAAGTTCACCATCTACAACAATATGTTCTGTGCTGGATTTCATGAGGGAGGGAGGGACTCCTGTCAGGGAGATTCTGGAGGCCCTCATGTGACAGAGGTGGAAGGCACCAGCTTCCTGACTGGCATCATCTCTTGGGGGGAGGAATGTGCTATGAAGGGGAAATATGGAATCTATACCAAGGTGTCCAGATATGTCAACTGGATCAAGGAGAAAACCAAGCTGACCTGA

In addition, two other variants were constructed. The first is a liveroptimized, Padua, 148T variant that is very similar to the above liveroptimized sequence, except it was synthesized using an alternate versionof the codon optimization algorithm.

Liver codon optimized fiX with Padua/Malmomutations and no CpG (version 2) (SEQ ID NO: 10)ATGCAGAGGGTGAACATGATCATGGCTGAGTCTCCTGGACTGATCACCATCTGCCTGCTGGGCTATCTGCTGTCTGCTGAGTGTACAGTGTTCCTGGACCATGAAAATGCTAATAAAATCCTGAACAGGCCAAAGAGGTACAATTCTGGGAAACTGGAGGAATTTGTGCAGGGAAACCTGGAGAGGGAATGCATGGAGGAAAAGTGTAGCTTTGAGGAAGCCAGGGAGGTGTTTGAAAATACAGAGAGGACCACAGAGTTCTGGAAACAGTATGTGGATGGGGATCAGTGTGAGTCCAACCCCTGTCTGAATGGAGGGTCTTGCAAGGATGATATCAACTCCTATGAGTGCTGGTGTCCTTTTGGATTTGAAGGCAAGAATTGTGAGCTGGATGTGACCTGTAACATCAAAAATGGGAGGTGTGAGCAGTTCTGTAAGAACTCTGCTGATAATAAAGTGGTCTGCAGCTGTACAGAAGGCTACAGGCTGGCTGAGAACCAGAAGAGCTGTGAACCAGCTGTGCCCTTCCCTTGTGGGAGGGTGTCTGTCAGCCAGACCAGCAAGCTGACCAGAGCTGAGACAGTGTTTCCTGATGTGGATTATGTCAACTCTACAGAGGCTGAAACCATCCTGGACAACATCACCCAGTCTACCCAGTCCTTCAATGACTTTACCAGGGTGGTGGGAGGGGAGGATGCTAAGCCAGGACAGTTCCCCTGGCAGGTGGTCCTGAATGGCAAAGTGGATGCTTTTTGTGGGGGCTCCATTGTGAATGAGAAGTGGATTGTCACAGCTGCTCACTGTGTGGAAACTGGGGTCAAGATCACAGTGGTGGCTGGAGAGCACAACATTGAGGAAACTGAACATACAGAGCAGAAAAGGAATGTGATCAGAATCATCCCCCACCATAACTACAATGCTGCTATCAACAAGTATAATCATGACATTGCCCTGCTGGAACTGGATGAGCCTCTGGTGCTGAACAGCTATGTCACCCCAATCTGCATTGCTGACAAGGAGTATACCAATATCTTCCTGAAATTTGGGTCTGGATATGTGTCTGGGTGGGGAAGGGTCTTCCACAAGGGAAGGTCTGCTCTGGTGCTGCAGTATCTGAGGGTGCCCCTGGTGGACAGAGCTACCTGCCTGCTGAGCACCAAGTTCACCATCTACAACAATATGTTCTGTGCTGGATTTCATGAGGGAGGGAGGGACTCCTGTCAGGGAGATTCTGGAGGCCCTCATGTGACAGAGGTGGAAGGCACCAGCTTCCTGACTGGCATCATCTCTTGGGGGGAGGAATGTGCTATGAAGGGGAAATATGGAATCTATACCAAGGTGTCCAGATATGTCAACTGGATCAAGGAGAAAACCAAGCTGACCTGA

In addition, a fiX sequence with Padua/Malmo mutations and no CpG wasoptimized according to the standard human codon optimization table (seeFIG. 2B).

Human codon optimized fIX with Padua/Malmo mutations and no CpG(SEQ ID NO: 127) ATGCAGAGGGTGAATATGATTATGGCTGAGTCCCCTGGGCTGATTACCATTTGCCTGCTGGGATACCTGCTGTCTGCTGAGTGTACAGTGTTCCTGGACCATGAGAATGCAAATAAGATCCTGAACAGGCCCAAAAGATATAATAGTGGAAAGCTGGAGGAATTTGTGCAGGGCAACCTGGAGAGAGAATGCATGGAGGAAAAGTGTAGCTTTGAGGAAGCCAGGGAGGTGTTTGAAAATACAGAGAGAACCACAGAATTCTGGAAGCAGTATGTGGATGGAGATCAGTGTGAGAGCAACCCCTGTCTGAATGGAGGGAGTTGCAAAGATGATATCAACTCATATGAATGCTGGTGTCCTTTTGGATTTGAAGGCAAAAATTGTGAGCTGGATGTGACCTGTAACATTAAGAATGGGAGGTGTGAGCAGTTTTGTAAAAACTCTGCTGATAATAAGGTGGTCTGCAGTTGTACAGAAGGGTATAGACTGGCTGAGAACCAGAAGTCCTGTGAACCAGCTGTGCCCTTCCCTTGTGGAAGGGTGTCTGTCTCCCAGACTTCAAAACTGACCAGAGCTGAGACTGTGTTTCCTGATGTGGATTATGTCAACAGCACAGAGGCTGAAACTATCCTGGACAACATTACTCAGTCTACCCAGAGTTTCAATGACTTTACCAGAGTGGTGGGAGGAGAGGATGCTAAACCAGGCCAGTTCCCCTGGCAGGTGGTCCTGAATGGGAAGGTGGATGCATTTTGTGGGGGATCTATTGTGAATGAGAAATGGATTGTCACAGCTGCTCACTGTGTGGAAACTGGGGTCAAGATCACAGTGGTGGCTGGAGAGCACAACATTGAGGAAACAGAACATACTGAGCAGAAGAGGAATGTGATCAGAATCATTCCTCACCATAACTACAATGCAGCCATCAACAAATATAATCATGACATTGCCCTGCTGGAACTGGATGAGCCTCTGGTGCTGAACAGCTATGTCACACCAATCTGCATTGCTGACAAGGAGTACACTAACATCTTCCTGAAGTTTGGGTCAGGATATGTGTCTGGATGGGGAAGAGTCTTCCACAAGGGCAGGTCTGCACTGGTGCTGCAGTATCTGAGAGTGCCTCTGGTGGATAGGGCCACTTGTCTGCTGTCTACCAAGTTCACCATCTACAACAATATGTTCTGTGCTGGATTTCATGAGGGAGGGAGAGACTCCTGTCAGGGAGATTCTGGAGGCCCACATGTGACAGAGGTGGAAGGCACCAGCTTCCTGACAGGCATCATTTCCTGGGGGGAGGAATGTGCAATGAAGGGGAAATATGGAATCTACACCAAAGTGAGCAGGTATGTGAACTGGATCAAGGAAAAGACCAAACTGACATGA

In vitro expression of the liver-optimized fIX sequence (SEQ ID NO: 10)and human-optimized fIX sequence (SEQ ID NO: 127) was assessed in HepG2cells transiently transfected with corresponding fVIII expressionplasmids (FIG. 7). The tissue specific optimization lead to increasedfiX activity in the HepG2 (hepatic) cells expressing the liver-optimizedfiX compared to human-optimized fiX. These results show that liveroptimization specifically benefits expression in hepatocyte derivedcells.

Example 2 Promoter Development

This example described the iterative development of optimized promotersequences for expression of protein in liver tissue and cells.

The promoters were synthesized de novo and cloned into an expressionplasmid driving the expression of clotting fVIII. FVIII activity wasmeasured 48 hours after transfection by one-stage clot assay. As acomparator, the hybrid liver promoter (HLP) was used. HLP represents oneof the shortest yet most powerful liver-directed promoters described todate. The HLP promoter and its use are described in McIntosh et al.,“Therapeutic levels of FVIII following a single peripheral veinadministration of rAAV vector encoding a novel human fVIII variant,”Blood, 25; 121(17):3335-44, 2013. The HLP sequence is provided as SEQ IDNO: 128:

TGTTTGCTGCTTGCAATGTTTGCCCATTTTAGGGTGGACACAGGACGCTGTGGTTTCTGAGCCAGGGGGCGACTCAGATCCCAGCCAGTGGACTTAGCCCCTGTTTGCTCCTCCGATAACTGGGGTGACCTTGGTTAATATTCACCAGCAGCCTCCCCCGTTGCCCCTCTGGATCCACTGCTTAAATACGGACGAGGACAGGGCCCTGTCTCCTCAGCTTCAGGCACCACCACTGACCTGGGACA GTGAATC

Initial Promoter Design (1^(st) Generation Promoters)

To begin construction of synthetic liver-directed promoters, two minimalliver directed promoters were selected that were designed platforms forfurther modification. These two promoters are designated as “ABP-SynO”(SEQ ID NO: 131) and “ABP-HP1-God”. These promoters are novel fusions ofpreviously described regulatory control elements. “ABP” is clusteredregion of transcription factor binding sites, “HP1” is a specifictranscription factor binding site, “God” is an enhancer-like region thatfunctions in direct proximity to the transcription start site, and“SynO” is a minimal promoter that contains the HP1 transcription factorbinding site and a TATA box. For all constructs, where not providedwithin the native context, a TATA sequence (TATAAA) was added orcompleted immediately 3′ to the promoter region.

Initial promoter designed were based on the “ABP” element, which isdescribed, for example, in Rouet et al., “A potent enhancer made ofclustered liver-specific elements in the transcription control sequencesof human alpha 1-microglobulin/bikunin gene,” J Biol Chem.,267(29):20765-73, 1992. ABP comprises the nucleotide sequence set forthas

ABP element (SEQ ID NO: 113):GTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAAs illustrated in FIG. 8, ABP comprises the following TF binding sites:HNF-1-1 (nucleotides 16-23 of SEQ ID NO: 4), HNF-4 (nucleotides 26-36 ofSEQ ID NO: 4), HNF-3a (nucleotides 39-45 of SEQ ID NO: 4), HNF1-2(nucleotides 48-62 of SEQ ID NO: 4), and HNF-3-2 TF (nucleotides 65-71of SEQ ID NO: 4).

Several of the disclosed promoters include an HP1 TF binding site(GTTAATAATTTTC, nucleotides 75-87 of SEQ ID NO: 4). The HP1 element isdescribed, for example, in Schorpp et al., “Hepatocyte-specific promoterelement HP1 of the Xenopus albumin gene interacts with transcriptionalfactors of mammalian hepatocytes,” J Mol Biol., 202(2):307-20, 1988. TheHP1 TF binding site is included in the SynO element (included in severalof the disclosed promoters), which also includes a TATA box. Thesequence of the SynO element is provided as

SynO element

(SEQ ID NO: 114) GAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAA

The SynO element is described, for example, in Ryffel et al., “Livercell specific gene transcription in vitro: the promoter elements HP1 andTATA box are necessary and sufficient to generate a liver-specificpromoter.” Nucleic Acids Res., 17(3): 939-953, 1989.

Several of the disclosed promoters include a “God” which comprises thesequence set forth as:

God element

(SEQ ID NO: 115) AGTCATATGTTTGCTCACTGAAGGTTACTAGTTAACAGGCATCCCTTAAACAGGAThe God element is described, for example, in Godbout et al., “Multipleregulatory elements in the intergenic region between thealpha-fetoprotein and albumin genes,” Mol Cell Biol., 6(2):477-87, 1986.

The ABP, SynO, and God elements were combined to form two novelpromoters, “ABP-SynO” and “ABP-HP1-God” as follows (see FIG. 8):

ABP-SynO promoter (SEQ ID NO: 131)GTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAA ABP-Hp1-God promoter(SEQ ID NO: 6) GTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAGAGGTTAATAATTTTCAGTCATATGTTTGCTCACTGAAGGTTACTAGTTAACAGGCATCCCTTAAACAGGATATAAAA

In vitro expression of FVIII was assayed in HepG2 cells transientlytransfected with FVIII expression plasmids driven by the ABP-SynO orABP-Hp1-God promoter (FIG. 9A). Additionally, In vivo fVIII activity inmice was assayed by hydrodynamically delivered naked plasmid expressingFVIII driven by the ABP-SynO or ABP-Hp1-God promoter (FIG. 9B). From theresults, it is shown that both the ABP-Syno and ABP-Hp1-God promotersdrive fVIII expression in vitro and in vivo. However, these initialdesigns do not drive fVIII expression as strongly as the HLP promoter invitro, and that the expression in vivo declines rapidly relative to HLP.

Initial Optimization (2^(nd) Generation Promoters)

In order to increase the transcriptional strength of the ABP-SynO andABP-Hp1-God promoters, multiple strategies for optimization werepursued. This includes altering the transcription factor binding sitesto reflect the consensus binding sequence, removing intervening spacebetween transcription factor binding sites, adding additionaltranscription factor binding sites, adding a transcription start sitemotif, and including the SV40 intron.

An ABP variant was generated that contains consensus TF binding sites,as follows:

ABP-exact (consensus transcription factor binding sites)(SEQ ID NO: 116) GTTAATCATTAACTTAAAAAGCAGTCAAAAGTCCAAAGGTCAAAGGTCAGAGCATTTACTCTCTCCAATGTTGACTCTCGTTAATGATTAAGGAGCAA TTGTTGACTTAs illustrated in FIG. 8, ABP-exact comprises the following consensus TFbinding sites: consensus HNF-1-1, consensus HNF-4, consensus HNF-3a,consensus HNF1-2, and consensus HNF-3-2. A condensed version ofApb-exact was generated that includes the same consensus TF bindingsites, but a shorter overall sequence, termed Short-ABP-exact, thesequence of which is set forth as:

Short-ABP-exact (SEQ ID NO: 117)GTTAATCATTAACTTAGGTCAAAGGTCAGACAATGTTGACTCTCGTTAATGATTAACCGGAATTGTTGACTT

The following features were further included in certain of the disclosedpromoters:

A transcription start site (TSS), which contains a 23 contains a GC richspacer and was placed immediately after a TATA box in the promoter foroptimal spacing with the transcription start motif immediately after thespacer (see FIG. 10). The TSS sequence assayed includes the sequence setforth as:

(nucleotides 116-146 of SEQ ID NO: 4) GCCAGCAGCAGCCTGACCACATCTCATCCTC

A HNF1a transcription factor binding site. HNF1a is a liver-directedtranscription factor:

(nucleotides 1-12 of SEQ ID NO: 4) GTTAATCATTAA

A Sp1 transcription factor binding site. Sp1 is a liver-directedtranscription factor:

(nucleotides 1-10 of SEQ ID NO: 121) TGGGCGGAGT

A SV40 intron sequence set forth as:

(nucleotides 163-225 of SEQ ID NO: 112)CTCTAAGGTAAATATAAAATTTTTAAGTGTATAATGTGTTAAACTACTGATTCTAATTGTTTGTGTATTTTAGATTCCAACCTATGGAACTGA

These elements were combined to form several novel promoters, as follows(see FIG. 11):

ABP-exact-SynO (SEQ ID NO: 118)GTTAATCATTAACTTAAAAAGCAGTCAAAAGTCCAAAGGTCAAAGGTCAGAGCATTTACTCTCTCCAATGTTGACTCTCGTTAATGATTAAGGAGCAATTGTTGACTTGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAA A ShortABP-exact-SynO(SEQ ID NO: 119) GTTAATCATTAACTTAGGTCAAAGGTCAGACAATGTTGACTCTCGTTAATGATTAACCGGAATTGTTGACTTGAGGTTAATAATTTTCCAGATCTCTCTG AGCAATAGTATAAAAABP-HP1-God-TSS (SEQ ID NO: 7)GTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAGAGGTTAATAATTTTCAGTCATATGTTTGCTCACTGAAGGTTACTAGTTAACAGGCATCCCTTAAACAGGATATAAAAGGCCAGCAGCAGCCTGACCACATCTCAT CCTC HNF1a-ABP-SynO(SEQ ID NO: 120) GTTAATCATTAAGTCGTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAA AA Sp1-ABP-SynO(SEQ ID NO: 121) TGGGCGGAGTGTCGTTAATTTTTAAAAAGCAGTCAAAAGTCCAAGTGGCCCTTGCGAGCATTTACTCTCTCTGTTTGCTCTGGTTAATAATCTCAGGAGCACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAHNF1-ShortABPExact-SynO-TSS-Int (SEQ ID NO: 112)GTTAATCATTAAGTCGTTAATCATTAACTTAGGTCAAAGGTCAGACAATGTTGACTCTCGTTAATGATTAACCGGAATTGTTGACTTGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTCCTCTAAGGTAAATATAAAATTTTTAAGTGTATAATGTGTTAAACTACTGATTCTAATTGTTTGTGTATTTTAGATTCCAACCTATGGA ACTGA

The promoters were synthesized de novo and cloned into an expressionplasmid driving the expression of clotting fVIII. FVIII activity wasmeasured 48 hours after transfection by one-stage clot assay. As acomparator, the hybrid liver promoter (HLP) is used in this and otherexperiments.

In vitro expression of FVIII was assayed in HepG2 cells transientlytransfected with FVIII expression plasmids driven by the respectivepromoter (FIG. 12A). Additionally, In vivo fVIII activity in mice wasassayed by hydrodynamically delivered naked plasmid expressing FVIIIdriven by the respective promoter (FIG. 12B). From these data, it isshown that the addition of the synthetic, novel, transcription startsite motif substantially improves expression. Further, the addition oftranscription factor binding sites outside of their native genomiccontext had unexpected and unpredicted impacts on expression. When addeddirectly proximal to the ABP enhancer element, the HNF1 and Sp1transcription factor binding sites completely abrogated expression. Whenthe HNF1 transcription factor binding site was added directly proximalto the shortABPExact enhancer, expression was robust. This findingillustrates that the complex spatiotemporal interactions oftranscription factors, in either their native or non-native genomiccontext, is difficult to model or predict. In addition, altering thetranscription factor binding sites to the consensus binding sequencesabrogated gene expression. However, the addition of the HNF1transcription factor binding site, transcription start site, and SV40intron was sufficient to rescue expression from HNF1 supplementedshortABPExact-SynO promoter design. As illustrated in FIG. 12B, theABP-Hp1-God-TSS and the HNF1-shortABPExact-SynO-TSS-Int both maintainedhigher expression than the HLP promoter over the course of theexperiment, showing that the addition of the transcription start site,HNF1 transcription factor binding site, adjustment of the ABP sequenceto the consensus sequence and removal of intervening DNA betweentranscription factor binding sites, and/or the addition of the SV40intron could improve the durability and strength of expression in vivo.

Further Optimization (3^(rd) Generation Promoters)

While the ABP-Hp1-God-TSS promoter design tested far exceeded thestrength of the HLP promoter, its size (204 bae pairs) remainedincompatible with some complete packaging of AAV-vectors, such as thosecontaining full-length containing fVIII transgenes. Further reduction inthe size of the promoter was targeted by selection of the most promisingelements tested and described above, as well as a novel element,shortABP, which is the ABP enhancer where the native genomictranscription factor binding site sequences are retained, but theintervening sequences between them have been truncated.

shortABP (nucleotides 16-71 of SEQ ID NO: 4):GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGA CAAACAAs illustrated in FIG. 13, shortABP contains the following TF bindingsites: HNF-1-1 (nucleotides 16-23 of SEQ ID NO: 4), HNF-4 (nucleotides26-36 of SEQ ID NO: 4), HNF-3a (nucleotides 39-45 of SEQ ID NO: 4),HNF1-2 (nucleotides 48-62 of SEQ ID NO: 4), and HNF-3-2 TF (nucleotides65-71 of SEQ ID NO: 4).

As illustrated in FIG. 13, the HNF1 TF binding site, the SynO element(containing a HP1 TF binding site and a TATA box), and a transcriptionstart site were linked to the shortABP to form theHNF1-shortABP-SynO-TSS (designated the Hepatic Combinatorial Bundle, orHCB), as follows:

HNF1-shortABP-SynO-TSS (also called HepaticCombinatorial Bundle, or HCB) (SEQ ID NO: 4)GTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC

As illustrated in FIG. 13, the HNF1 TF binding site, the God element, aTATA box, and a transcription start site were linked to the shortABP toform the shortABP-HP1-God-TSS, as follows:

shortABP-HP1-God-TSS  (SEQ ID NO: 5)GTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACATACATTTTCAGTCATATGTTTGCTCACTGAAGGTTACTAGTTAACAGGCATCCCTTAAACAGGATATAAAAGGCCAGCAGCAGCCTGACCACAT CTCATCCTC

The promoters were synthesized de novo and cloned into an expressionplasmid driving the expression of clotting fVIII. FVIII activity wasmeasured 48 hours after transfection by one-stage clot assay. In vitroexpression of FVIII was assayed in HepG2 cells transiently transfectedwith FVIII expression plasmids driven by the respective promoter isshown in FIG. 14A. Additionally, In vivo fVIII activity in mice wasassayed by hydrodynamically delivered naked plasmid expressing FVIIIdriven by the respective promoter (FIG. 14). From these data, it isshown that the HNF1-shortABP-SynO-TSS promoter (HCB) promotes increasedexpression of fVIII compared to that of HLP both in vivo and in vitro,while maintaining durable expression 4-14 fold greater than that of HLPin vivo, despite the HNF1-shortABP-SynO-TSS being 42% smaller than HLP.

Supplemental Optimization (4^(th) Generation Promoters)

A powerful, liver-directed enhancer, designated the hepatocyte specificcomputational regulatory module (HSCRM8 or “HS”) was recentlyconstructed by combining the sequences from several species into acomputationally constructed novel enhancer (see, e.g., Nair et al.,“Computationally designed liver-specific transcriptional modules andhyperactive fIX improve hepatic gene therapy,” Blood, 23(20): 3195-3199,2014). The sequence of the HS enhancer and corresponding transcriptionfactor binding sites are provided as follows:

HS (HSCRM8 non-human enhancer sequence) (SEQ ID NO: 101)GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGA GCAAACAGGGACTAAGTCCACThe HS response element includes the following TF binding sites:

MY-OD GGCTGCTGGTGAAT-ATT, nucleotides 5-22 of SEQ ID NO: 101 CEBPGCTGCTGGTGAA, nucleotides 7-18 of SEQ ID NO: 101 Nhf1GCTGGTGAATATTAACCA, nucleotides 10-27 of SEQ ID NO: 101 Lef1/TCF1TTAACCAAGGT, nucleotides 21-31 of SEQ ID NO: 101 CEBPCGGAGGAGCAAA, nucleotides 44-55 of SEQ ID NO: 101 ForkheadGGAGCAAACAGGG, nucleotides 48-60 of SEQ ID NO: 101 Lef1/TCF1AGGGACTAAG, nucleotides 57-66 of SEQ ID NO: 101

The human genome was examined to determine human sequences correspondingto those of the HS element and the HS element was modified to containonly human sequences to generate a fully human enhancer sequence termed“HSh.” The sequence of the HSh enhancer and corresponding transcriptionfactor binding sites are provided as follows (see also, FIG. 15):

HSh (human genomic sequence) (SEQ ID NO: 111)GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGA GCAAACAGGGGCTAAGTCCACThe HSh response element includes the following TF binding sites:

MYOD GGCTGCTGGTGAATATT, nucleotides 5-22 of SEQ ID NO: 101 CEBPGCTGCTGGTGAA, nucleotides 7-18 of SEQ ID NO: 101 Nhf1GCTGGTGAATATTAACCA, nucleotides 10-27 of SEQ ID NO: 101 Lef1/TCF1TTAACCAAGGT, nucleotides 21-31 of SEQ ID NO: 101 CEBPCGGAGGAGCAAA, nucleotides 44-55 of SEQ ID NO: 101 ForkheadGGAGCAAACAGGG, nucleotides 48-60 of SEQ ID NO: 101 Lef1/TCF1AGGGGCTAAG, nucleotides 57-66 of SEQ ID NO: 111Portions of the HSh enhancer were also utilized, as follows:

5′HSh (5′ portion of HSCRM8h) (nucleotides 6-32 of SEQ ID NO: 111)GGCTGCTGGTGAATATTAACCAAGGTCThe 5′HSh response element includes the following TF binding sites:

MYOD GGCTGCTGGTGAATATT, nucleotides 5-22 of SEQ ID NO: 101 CEBPGCTGCTGGTGAA, nucleotides 7-18 of SEQ ID NO: 101 Nhf1GCTGGTGAATATTAACCA, nucleotides 10-27 of SEQ ID NO: 101 Lef1/TCF1TTAACCAAGGT, nucleotides 21-31 of SEQ ID NO: 1013′HSh (3′ portion of HSCRM8h) (nucleotides 44-68 of SEQ ID NO: 111)CGGAGGAGCAAACAGGGGCTAAGTCThe 3′HSh response element includes the following TF binding sites:

CEBP CGGAGGAGCAAA, nucleotides 44-55 of SEQ ID NO: 101 ForkheadGGAGCAAACAGGG, nucleotides 48-60 of SEQ ID NO: 101 Lef1/TCF1AGGGGCTAAG nucleotides 57-66 of SEQ ID NO: 111sHS (short HS, the intervening space between the 5′ and 3′ clusters oftranscription factor binding sites has been removed) (nucleotides 1-54of SEQ ID NO: 106)

GGCTGCTGGTGAATATTAACCAAGGTCATCGGAGGAGCAAACAGGGACT AAGTCThe sHS response element includes the following TF binding sites:

MYOD GGCTGCTGGTGAATATT, nucleotides 5-22 of SEQ ID NO: 101 CEBPGCTGCTGGTGAA, nucleotides 7-18 of SEQ ID NO: 101 Nhf1GCTGGTGAATATTAACCA, nucleotides 10-27 of SEQ ID NO: 101 Lef1/TCF1TTAACCAAGGT, nucleotides 21-31 of SEQ ID NO: 101 CEBPCGGAGGAGCAAA, nucleotides 44-55 of SEQ ID NO: 101 ForkheadGGAGCAAACAGGG, nucleotides 48-60 of SEQ ID NO: 101 Lef1/TCF1AGGGACTAAG, nucleotides 57-66 of SEQ ID NO: 111

Additionally, a modified form of the short ABP promoter, termed“supershortABP” was constructed by further deleting nucleotides andrearranging TF binding sites. The sequence of the supershort ABPresponse element and corresponding transcription factor binding sitesare provided as follows:

Super short ABP (further shortened ABP-based element) (SEQ ID NO: 122)

CCCTTGCTGGTTAATAATCTCAGTTAATTTGTTTGCACAAACAThe supershort ABP response element include the following TF bindingsites:

HNF4 CCCTTGC, nucleotides 1-7 of SEQ ID NO: 122 HNF1bTGGTTAATAATCTCA, nucleotides 8-22 of SEQ ID NO: 122 HNF1GTTAATT, nucleotides 23-29 of SEQ ID NO: 122 HNF3TGTTTGC, nucleotides 30-36 of SEQ ID NO: 122 HNF3bACAAACA, nucleotides 37-43 of SEQ ID NO: 122

As illustrated in FIG. 16, the above elements were combined to formseveral novel promoters, as follows (see FIG. 11):

Agro (SEQ ID NO: 107) GGCTGCTGGTGAATATTAACCAAGGTCCCCTTGCTGGTTAATAATCTCAGTTAATTTGTTTGCACAAACACGGAGGAGCAAACAGGGGAGGTTAATAATTTTCTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC

The Agro sequence includes 5′HS (nucleotides 1-27 of SEQ ID NO: 107),Super short ABP (nucleotides 28-70 of SEQ ID NO: 107), 3′HSh(nucleotides 71-87 of SEQ ID NO: 107), SynO (nucleotides 88-110 of SEQID NO: 107), and TSS (nucleotides 111-142 of SEQ ID NO: 107)

HSh-HCB (SEQ ID NO: 102)GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGAGCAAACAGGGGCTAAGTCCACTAGGTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC 5′HSh-HCB (SEQ ID NO: 104)GGCTGCTGGTGAATATTAACCAAGGTCGTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC 3′HSh-HCB (SEQ ID NO: 103)CGGAGGAGCAAACAGGGGCTAAGTCGTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC HSh-SynO-TSS (SEQ ID NO: 105)GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGAGCAAACAGGGGCTAAGTCCACGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC HS-SynO-TSS(SEQ ID NO: 108) GGGGAGGCTGCTGGTGAATATTAACCAAGGTCACCCCAGTTATCGGAGGAGCAAACAGGGACTAAGTCCACGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC sHS-SynO-TSS(SEQ ID NO: 106) GGCTGCTGGTGAATATTAACCAAGGTCATCGGAGGAGCAAACAGGGACTAAGTCGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTC

The promoters were synthesized de novo and cloned into an expressionplasmid driving the expression of clotting fVIII. FVIII activity wasmeasured 48 hours after transfection by one-stage clot assay. In vitroexpression of FVIII was assayed in HepG2 cells transiently transfectedwith FVIII expression plasmids driven by the respective promoter isshown in FIG. 17. These results demonstrate that the in vivo strength ofthe HCB promoter can be augmented by the addition of a supplementalenhancer sequences. The greatest benefit was seen when the complete,human, HSh enhancer was added to the 5′ end of the HCB promoter.Supplementing only the 5′ or 3′ portions of the HSh attenuated theimproved expression slightly compared to the complete HSh module.Additionally, when the shortABP enhancer was removed from the HCB designand instead replaced with either HSh or HS enhancers, fVIII expressiondeclined slightly from the levels seen in the HSh-HCB promoter, whichcontains the shortABP-enhancer. However, when the sHS-SynO plasmid wasadministered hydrodynamically to mice, no expression was observed,showing that the shortABP enhancer module may be a more suitableenhancer for durable in vivo expression.

Example 3 Recombinant AAV Vector for fVIII Expression

This example illustrates exemplary recombinant AAV vectors encoding afVIII variant that comprise a genome sized for optimal AAV vector-basedprotein expression (that is, a genome of 5 kb or fewer bp).

FIG. 4 depicts AAV-based vectors for expression of fVIII variants thatlack the B-domain. However, the constructs shown in FIG. 4 are above the5.0 kb limit for optimal protein expression from an AAV vector. Removingnonessential viral genomic DNA and cloning remnants, and substitutingshorter promoter sequences (such as the HCB promoter (SEQ ID NO: 4, 146bp), enabled the development of a high expression fVIII-AAV genome ofapproximately 4.9 kb in length.

An exemplary AAV vector with such a genome is depicted in FIG. 18. Thisfigure illustrates an AAV vector including 5′ and 3′ ITRs, the HCB (SEQID NO: 4) promoter, a nucleic acid molecule encoding a variant fVIIIprotein that lacks the B-domain (such as any one of the ET3 or HSQCpG-depleted and liver codon optimized sequences provided herein), and asynthetic poly A sequence.

An exemplary sequence of an AAV cassette as shown in FIG. 18 is providedas SEQ ID NO: 129, which has the following structure:

(5′AAV2 ITR)-RE-(HCB Promoter)-Kozak-(HSQ coding region)-RE-(polyadenylation signal)-RE-(3′AAV2 ITR)The elements of the AAV cassette of SEQ ID NO: 129 are as follows:

Element Start (bp) End (bp) 5′ AAV2 ITR  1  141 AgeI (restriction site) 142  147 HCB promoter  148  293 Destroyed XhoI site  294  299 Kozakconsensus sequence  300  304 Liver optimized HSQ with CpGs  305 4678NotI (restriction site) 4679 4686 Rabbit beta globin polyA signal 46874735 MunI (restriction site) 4736 4741 3′ AAV2 ITR 4742 4882

The restriction sites can optionally be removed from the cassette toprovide a shortened recombinant AAV genome. Additionally, the transgenecan be substituted as needed. Removing the restriction sites elementswould generate a vector of 4885 base pairs (ET3) or 4855 (HSQ).

SEQ ID NO: 129: CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCAAAGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGCGCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTACCGGTGTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTCGTCGAGCCACCATGCAGATCGAACTGTCTACCTGTTTCTTTCTGTGCCTGCTGCGGTTTTGTTTTTCCGCTACCAGAAGATACTACCTGGGAGCCGTCGAACTGAGCTGGGATTACATGCAGTCTGACCTGGGAGAGCTGCCCGTGGACGCTAGATTCCCACCTAGAGTCCCTAAGTCCTTCCCCTTCAACACCAGCGTGGTCTACAAGAAAACCCTGTTCGTGGAGTTTACCGACCACCTGTTCAACATCGCTAAGCCTAGACCACCATGGATGGGACTGCTGGGACCAACCATCCAGGCCGAGGTGTACGACACCGTGGTCATCACCCTGAAAAACATGGCTTCTCACCCCGTGTCCCTGCATGCTGTGGGCGTCTCCTACTGGAAGGCCAGCGAAGGGGCTGAGTATGACGATCAGACCAGCCAGCGGGAAAAAGAGGACGATAAGGTGTTCCCTGGCGGGTCCCATACCTACGTGTGGCAGGTCCTGAAGGAGAATGGACCAATGGCTTCCGACCCTCTGTGCCTGACCTACTCTTATCTGTCCCACGTGGACCTGGTCAAGGATCTGAACAGCGGCCTGATCGGGGCTCTGCTGGTGTGTCGCGAAGGGTCCCTGGCCAAGGAGAAAACCCAGACCCTGCATAAGTTCATCCTGCTGTTCGCCGTGTTTGACGAAGGAAAAAGCTGGCACTCTGAGACCAAGAACTCTCTGATGCAGGACAGGGATGCCGCTTCCGCCAGAGCTTGGCCCAAGATGCACACCGTGAACGGCTACGTCAATAGGAGCCTGCCTGGACTGATCGGCTGCCACAGAAAGTCCGTGTATTGGCATGTCATCGGAATGGGCACCACCCCTGAAGTGCACAGCATCTTCCTGGAGGGGCATACCTTTCTGGTCCGCAACCACCGGCAGGCTAGCCTGGAGATCTCTCCAATCACCTTCCTGACCGCCCAGACCCTGCTGATGGACCTGGGACAGTTCCTGCTGTTTTGCCACATCTCCAGCCACCAGCATGATGGCATGGAGGCTTACGTGAAAGTCGACTCCTGTCCCGAGGAACCTCAGCTGAGGATGAAGAACAATGAGGAAGCCGAAGACTATGACGATGACCTGACCGACAGCGAGATGGATGTGGTCCGCTTCGATGACGATAACTCTCCCTCCTTTATCCAGATCCGGTCCGTGGCCAAGAAACACCCTAAGACCTGGGTCCATTACATCGCCGCTGAGGAAGAGGACTGGGATTATGCTCCACTGGTGCTGGCCCCCGACGATAGATCCTACAAAAGCCAGTATCTGAACAATGGACCCCAGAGGATCGGCAGAAAGTACAAGAAAGTGAGGTTCATGGCTTATACCGATGAGACCTTTAAGACCAGAGAAGCCATCCAGCACGAGTCCGGGATCCTGGGACCTCTGCTGTACGGCGAAGTGGGGGACACCCTGCTGATCATCTTCAAGAACCAGGCCAGCAGGCCTTACAATATCTATCCACATGGCATCACCGATGTGAGACCTCTGTACTCCCGCCGGCTGCCAAAGGGCGTGAAACACCTGAAGGACTTCCCAATCCTGCCCGGGGAAATCTTTAAGTATAAATGGACCGTCACCGTCGAGGATGGGCCCACCAAGAGCGACCCTAGGTGCCTGACCAGATACTATTCTTCCTTCGTGAATATGGAGAGAGACCTGGCTTCCGGACTGATCGGACCCCTGCTGATCTGTTACAAAGAGAGCGTGGATCAGCGCGGCAACCAGATCATGTCTGACAAGCGGAATGTGATCCTGTTCAGCGTCTTTGACGAAAACCGCTCTTGGTACCTGACCGAGAACATCCAGCGGTTCCTGCCTAATCCAGCTGGAGTGCAGCTGGAAGATCCCGAGTTCCAGGCCTCTAACATCATGCATTCCATCAATGGCTACGTGTTCGACTCCCTGCAGCTGAGCGTGTGCCTGCACGAGGTCGCTTACTGGTATATCCTGAGCATCGGAGCCCAGACCGATTTCCTGTCTGTGTTCTTTTCCGGCTACACCTTTAAGCATAAAATGGTGTATGAGGACACCCTGACCCTGTTCCCATTTTCCGGCGAAACCGTGTTCATGAGCATGGAGAATCCCGGGCTGTGGATCCTGGGATGCCACAACTCCGATTTCAGGAATAGAGGGATGACCGCCCTGCTGAAAGTGAGCTCTTGTGACAAGAACACCGGAGACTACTATGAAGATAGCTACGAGGACATCTCTGCTTATCTGCTGTCCAAAAACAATGCCATCGAGCCCAGGAGCTTCTCTCAGAACCCTCCAGTGCTGAAGCGCCACCAGCGGGAGATCACCAGAACCACCCTGCAGAGCGATCAGGAAGAGATCGACTACGACGATACCATCTCCGTGGAAATGAAGAAAGAGGACTTCGATATCTATGACGAAGATGAGAACCAGTCTCCCAGGTCCTTCCAGAAGAAAACCAGACATTACTTTATCGCCGCTGTGGAGCGGCTGTGGGACTATGGCATGTCCAGCTCTCCTCACGTGCTGAGAAATAGAGCTCAGTCCGGAAGCGTCCCACAGTTCAAGAAAGTGGTCTTCCAGGAGTTTACCGACGGAAGCTTTACCCAGCCACTGTACCGCGGCGAACTGAACGAGCACCTGGGGCTGCTGGGACCCTATATCCGGGCTGAAGTGGAGGATAACATCATGGTCACCTTCAGGAATCAGGCCAGCAGACCCTACTCTTTTTATTCCAGCCTGATCTCCTACGAAGAGGACCAGAGACAGGGAGCTGAACCAAGAAAAAACTTCGTGAAGCCTAATGAGACCAAAACCTACTTTTGGAAGGTGCAGCACCATATGGCCCCTACCAAAGACGAGTTCGATTGCAAGGCCTGGGCTTATTTTAGCGACGTGGATCTGGAGAAGGACGTCCACTCCGGCCTGATCGGGCCACTGCTGGTGTGTCATACCAACACCCTGAATCCAGCTCACGGAAGGCAGGTGACCGTCCAGGAATTCGCCCTGTTCTTTACCATCTTTGATGAGACCAAGAGCTGGTACTTCACCGAAAACATGGAGAGGAATTGCAGAGCCCCATGTAACATCCAGATGGAAGACCCCACCTTCAAGGAGAACTACAGATTTCATGCTATCAATGGGTATATCATGGATACCCTGCCAGGACTGGTCATGGCTCAGGACCAGAGGATCAGATGGTACCTGCTGAGCATGGGGTCTAACGAGAATATCCACTCCATCCATTTCAGCGGACACGTGTTTACCGTCCGCAAGAAAGAAGAGTACAAGATGGCCCTGTACAACCTGTATCCCGGCGTGTTCGAAACCGTCGAGATGCTGCCTTCCAAGGCTGGGATCTGGCGGGTGGAATGCCTGATCGGGGAGCACCTGCATGCCGGAATGTCTACCCTGTTCCTGGTGTACTCCAATAAGTGTCAGACCCCCCTGGGGATGGCTAGCGGACATATCCGCGACTTCCAGATCACCGCTTCCGGACAGTACGGACAGTGGGCTCCTAAGCTGGCTAGACTGCACTATTCTGGCTCCATCAACGCTTGGTCTACCAAAGAGCCTTTCTCCTGGATCAAGGTGGACCTGCTGGCTCCAATGATCATCCATGGCATCAAAACCCAGGGGGCCAGGCAGAAGTTCTCTTCCCTGTACATCAGCCAGTTTATCATCATGTATTCTCTGGATGGGAAGAAATGGCAGACCTACAGAGGCAATTCCACCGGGACCCTGATGGTGTTCTTTGGCAACGTCGACAGCTCTGGGATCAAGCACAACATCTTCAATCCCCCTATCATCGCCCGCTACATCCGGCTGCACCCAACCCATTATTCCATCCGCAGCACCCTGCGGATGGAGCTGATGGGGTGCGATCTGAACAGCTGTTCTATGCCCCTGGGAATGGAGTCTAAGGCCATCTCCGACGCTCAGATCACCGCCTCCAGCTACTTCACCAATATGTTTGCTACCTGGTCCCCAAGCAAGGCTAGACTGCATCTGCAGGGAAGAAGCAACGCTTGGAGACCACAGGTGAACAATCCCAAGGAGTGGCTGCAGGTCGACTTCCAGAAAACCATGAAGGTGACCGGAGTCACCACCCAGGGCGTGAAAAGCCTGCTGACCTCTATGTACGTCAAGGAGTTCCTGATCTCTTCCAGCCAGGACGGGCACCAGTGGACCCTGTTCTTTCAGAACGGAAAGGTGAAAGTCTTCCAGGGCAATCAGGATTCCTTTACCCCTGTGGTCAACAGCCTGGACCCACCCCTGCTGACCAGGTACCTGAGAATCCACCCACAGTCCTGGGTGCATCAGATCGCTCTGAGGATGGAAGTCCTGGGCTGCGAGGCCCAGGACCTGTATTGAGCGGCCGCAATAAAATATCTTTATTTTCATTACATCTGTGTGTTGGTTTTTTGTGTGCAATTGAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGCCCGGGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAGCGCGCAGCTGC CTGCAGG

Another exemplary AAV vector including a fVIII transgene driven by theHCB promoter is provided as SEQ ID NO: 130, which provides aprototypical design of an AAV cassette encoding a therapeutic transgeneunder control of the HCB promoter. Each element is separated by one ortwo restriction enzyme (RE) sites, which allow for easy substitution ofthese elements. In SEQ ID NO: 130, the order of elements is as follows:

(5′ AAV2 ITR)-RE-(HCB Promoter)-RE-(MVM Intron)-RE-Kozak-(ET3 codingregion)-RE-(poly adenylation signal)-RE-(3′ AAV2 ITR)

AAV2-HCB-ET3-LCO-NCG-SpA

Element Start (bp) End (bp) 5′ AAV2 ITR   1  141 AgeI (restriction site) 142  147 HCB promoter  148  293 SalI + PacI (restriction sites)  294 307 MVM intron  308  399 XhoI (restriction site)  400  405 Kozakconsensus sequence  406  410 Liver optimized ET3 no CpGs  411 4814 NotI(restriction site) 4815 4822 Rabbit beta globin polyA signal 4823 4871MunI (restriction site) 4872 4877 3′ AAV2 ITR 4878 5018

The intron and restriction sites can optionally be removed from thecassette to provide a shortened recombinant AAV genome. Additionally,the transgene can be substituted as needed. Removing the intron andrestriction sites elements would generate a vector of 4885 base pairs(ET3) or 4855 (HSQ).

AAV2-HCB-ET3-LCO-NCG-SpA virus particles were generated and used totransduce mice. fVIII activity in serum was assayed at various timepoint post-transduction (see FIG. 19). The in vivo gene therapy assaywas performed substantially as described in Brown et al. (“BioengineeredFactor FVIII Enables Long-Term Correction of Murine Hemophilia AFollowing Liver-Directed Adeno-Associated Viral Vector Delivery,”Molecular Therapy—Methods and Clinical Development. 1:14036, 2014).

SEQ ID NO: 130: CCTGCAGGCAGCTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCAAAGCCCGGGCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGCGCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTACCGGTGTTAATCATTAAGTCGTTAATTTTTGTGGCCCTTGCGATGTTTGCTCTGGTTAATAATCTCAGGACAAACAGAGGTTAATAATTTTCCAGATCTCTCTGAGCAATAGTATAAAAGGCCAGCAGCAGCCTGACCACATCTCATCCTCGTCGACTTAATTAAAAGAGGTAAGGGTTTAAGGGATGGTTGGTTGGTGGGGTATTAATGTTTAATTACCTGGAGCACCTGCCTGAAATCACTTTTTTTCAGGTTGGCTCGAGCCACCATGCAGCTGGAACTGTCTACCTGTGTGTTTCTGTGTCTGCTGCCTCTGGGGTTTTCTGCTATCAGGAGATACTATCTGGGAGCTGTGGAGCTGTCCTGGGACTACAGGCAGTCTGAGCTGCTGAGAGAACTGCATGTGGATACCAGATTCCCAGCTACAGCTCCAGGAGCTCTGCCTCTGGGCCCATCTGTGCTGTACAAGAAAACAGTCTTTGTGGAGTTTACAGACCAGCTGTTCTCTGTGGCCAGGCCAAGACCACCTTGGATGGGACTGCTGGGACCAACCATCCAGGCTGAGGTGTATGATACAGTGGTGGTGACCCTGAAAAACATGGCCTCCCATCCTGTGAGCCTGCATGCTGTGGGGGTGTCCTTCTGGAAGTCCTCTGAGGGAGCTGAGTATGAAGACCATACCTCCCAGAGGGAGAAAGAAGATGATAAGGTGCTGCCTGGCAAAAGCCAGACCTATGTCTGGCAGGTGCTGAAGGAGAATGGACCAACTGCTTCTGACCCACCATGCCTGACCTACTCTTATCTGTCCCATGTGGATCTGGTGAAGGACCTGAATTCTGGACTGATTGGAGCTCTGCTGGTGTGTAGAGAGGGAAGCCTGACCAGAGAAAGAACCCAGAACCTGCATGAGTTTGTCCTGCTGTTTGCTGTGTTTGATGAAGGGAAGAGCTGGCACTCTGCCAGGAATGACTCCTGGACCAGAGCTATGGATCCAGCTCCTGCTAGAGCTCAGCCTGCTATGCACACAGTCAATGGCTATGTGAATAGGTCTCTGCCAGGACTGATTGGCTGCCATAAGAAATCTGTCTATTGGCATGTGATTGGAATGGGCACCAGCCCTGAGGTGCATTCTATCTTCCTGGAAGGCCACACCTTTCTGGTCAGGCACCATAGACAGGCCTCTCTGGAGATCTCCCCTCTGACCTTCCTGACAGCTCAGACCTTTCTGATGGACCTGGGGCAGTTCCTGCTGTTTTGCCATATCTCTTCCCACCATCATGGAGGAATGGAGGCTCATGTCAGGGTGGAATCCTGTGCTGAGGAACCACAGCTGAGAAGAAAGGCTGATGAGGAAGAGGACTATGATGATAACCTGTATGACTCTGATATGGATGTGGTGAGGCTGGATGGGGATGATGTCAGCCCTTTCATCCAGATCAGGTCTGTGGCCAAGAAACATCCAAAGACCTGGGTCCACTACATTGCTGCTGAAGAGGAAGATTGGGACTATGCCCCCCTGGTGCTGGCTCCTGATGATAGATCCTACAAAAGCCAGTATCTGAACAATGGGCCCCAGAGGATTGGAAGGAAGTACAAGAAAGTGAGGTTCATGGCCTATACAGATGAGACCTTTAAGACCAGAGAGGCTATCCAGCATGAATCTGGGATCCTGGGACCTCTGCTGTATGGAGAAGTGGGGGATACCCTGCTGATCATCTTCAAGAACCAGGCCTCCAGGCCATACAATATCTATCCCCATGGCATCACAGATGTGAGACCACTGTACAGCAGGAGACTGCCCAAGGGGGTCAAACACCTGAAGGATTTCCCCATCCTGCCTGGAGAGATCTTTAAGTATAAATGGACAGTCACAGTGGAAGATGGGCCTACCAAGTCTGATCCAAGGTGCCTGACCAGATACTATAGCTCTTTTGTGAACATGGAGAGAGACCTGGCTTCTGGACTGATTGGACCCCTGCTGATCTGTTACAAAGAGTCTGTGGACCAGAGGGGCAACCAGATCATGTCTGATAAGAGAAATGTCATCCTGTTCTCTGTGTTTGATGAGAACAGGAGCTGGTACCTGACAGAGAACATCCAGAGGTTCCTGCCAAATCCAGCTGGAGTGCAGCTGGAGGACCCAGAATTTCAGGCTTCCAACATCATGCATAGCATCAATGGCTATGTGTTTGATAGCCTGCAGCTGTCTGTCTGCCTGCATGAGGTGGCCTACTGGTATATCCTGTCCATTGGAGCTCAGACAGACTTCCTGTCTGTGTTCTTTAGTGGGTACACCTTTAAGCATAAAATGGTGTATGAGGATACCCTGACCCTGTTCCCCTTTTCTGGGGAGACAGTGTTCATGTCCATGGAAAACCCTGGCCTGTGGATCCTGGGGTGCCACAACTCTGACTTCAGGAATAGAGGAATGACAGCCCTGCTGAAAGTGTCCAGCTGTGATAAGAATACAGGGGATTACTATGAGGACTCTTATGAAGATATCTCTGCTTATCTGCTGAGCAAGAACAATGCCATTGAGCCCAGGTCTTTTGCTCAGAACTCCAGACCTCCATCTGCTTCTGCTCCTAAGCCACCTGTGCTGAGAAGACATCAGAGGGACATCTCCCTGCCTACCTTCCAGCCAGAGGAAGATAAAATGGACTATGATGATATCTTCAGCACAGAGACCAAGGGGGAAGATTTTGACATCTATGGAGAGGATGAAAACCAGGATCCAAGATCCTTCCAGAAGAGAACCAGACACTACTTTATTGCTGCTGTGGAGCAGCTGTGGGACTATGGGATGTCTGAAAGCCCAAGGGCCCTGAGGAACAGAGCTCAGAATGGAGAGGTGCCCAGATTCAAGAAAGTGGTGTTCAGAGAGTTTGCTGATGGCAGCTTTACCCAGCCATCTTACAGGGGGGAGCTGAACAAGCATCTGGGGCTGCTGGGACCCTATATCAGAGCTGAGGTGGAAGATAACATCATGGTGACCTTCAAGAATCAGGCTTCTAGGCCCTACTCCTTTTATTCTTCCCTGATCTCCTACCCTGATGATCAGGAGCAGGGAGCTGAACCTAGGCACAACTTTGTGCAGCCAAATGAGACCAGAACCTACTTTTGGAAGGTGCAGCATCACATGGCTCCCACAGAGGATGAATTTGACTGCAAAGCTTGGGCCTATTTTTCTGATGTGGACCTGGAGAAGGATGTGCATTCTGGCCTGATTGGGCCTCTGCTGATCTGTAGGGCCAACACCCTGAATGCTGCTCATGGAAGACAGGTCACAGTGCAGGAGTTTGCTCTGTTCTTTACCATCTTTGATGAAACCAAGAGCTGGTACTTCACAGAGAATGTGGAAAGGAATTGCAGAGCCCCCTGTCATCTGCAGATGGAGGACCCTACCCTGAAGGAAAACTACAGGTTCCATGCCATCAATGGATATGTCATGGATACCCTGCCTGGCCTGGTCATGGCTCAGAACCAGAGGATCAGATGGTACCTGCTGTCTATGGGATCCAATGAGAATATCCATAGCATCCACTTCTCTGGCCATGTCTTTTCTGTGAGGAAGAAAGAGGAATACAAAATGGCTGTGTACAATCTGTATCCTGGGGTCTTTGAGACAGTGGAAATGCTGCCAAGCAAAGTGGGAATCTGGAGAATTGAGTGCCTGATTGGGGAACACCTGCAGGCTGGGATGAGCACCACCTTCCTGGTGTACTCTAAGAAATGTCAGACCCCACTGGGGATGGCCTCTGGACATATCAGGGACTTCCAGATCACAGCTTCTGGACAGTATGGACAGTGGGCTCCAAAGCTGGCTAGACTGCACTATTCTGGCTCCATCAATGCCTGGTCTACCAAAGAGCCATTCTCCTGGATCAAGGTGGACCTGCTGGCCCCCATGATCATCCATGGAATCAAAACCCAGGGAGCTAGGCAGAAGTTCAGCTCTCTGTACATCTCCCAGTTTATCATCATGTATAGCCTGGATGGGAAGAAATGGCAGACCTACAGAGGCAATTCCACTGGGACCCTGATGGTCTTCTTTGGAAATGTGGATTCCTCTGGCATCAAGCACAACATCTTCAATCCACCCATCATTGCCAGGTACATCAGGCTGCATCCTACCCACTATAGCATCAGGTCTACCCTGAGAATGGAGCTGATGGGATGTGACCTGAACAGCTGTTCTATGCCACTGGGCATGGAGTCCAAGGCTATCTCTGATGCCCAGATCACAGCTTCTTCCTACTTCACCAATATGTTTGCTACCTGGTCCCCAAGCAAGGCTAGACTGCACCTGCAGGGAAGATCCAATGCTTGGAGACCCCAGGTGAACAATCCTAAGGAGTGGCTGCAGGTGGACTTCCAGAAAACCATGAAGGTCACAGGGGTGACCACCCAGGGAGTGAAATCTCTGCTGACCTCCATGTATGTCAAGGAGTTCCTGATCAGCTCTTCCCAGGATGGCCACCAGTGGACCCTGTTCTTTCAGAATGGCAAGGTCAAAGTGTTCCAGGGGAATCAGGACTCTTTTACCCCAGTGGTGAACTCCCTGGATCCTCCACTGCTGACCAGGTACCTGAGAATCCATCCTCAGAGCTGGGTGCACCAGATTGCTCTGAGAATGGAGGTCCTGGGATGTGAAGCTCAGGACCTGTATTGAGCGGCCGCAATAAAATATCTTTATTTTCATTACATCTGTGTGTTGGTTTTTTGTGTGCAATTGAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGCGCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCCGACGCCCGGGCTTTGCCCGGGCGGCCTCAGTGAG CGAGCGAGCGCGCAGCTGCCTGCAGG

Example 4 Treatment of Human Hemophilia a Using AAV-Based Gene Therapy

This example describes an exemplary method for the clinical use of AAVvectors encoding fVIII for the treatment of hemophilia A.

A patient diagnosed with hemophilia A is selected for treatment. Thepatient is administered a therapeutically effective amount of arecombinant AAV encoding the ET3 or HSQ fVIII variant, such as AAV-ET3or AAV-HSQ under control of a HCB promoter as disclosed herein. Therecombinant AAV can be administered intravenously. An appropriatetherapeutic dose can be selected by a medical practitioner. In somecases, the therapeutically effective dose is in the range of 1×10″ to1×10¹⁴ viral particles (vp)/kg, such as about 1×10¹² vp/kg. In mostinstances, the patient is administered a single dose. The health of thesubject can be monitored over time to determine the effectiveness of thetreatment.

It will be apparent that the precise details of the methods orcompositions described may be varied or modified without departing fromthe spirit of the described embodiments. We claim all such modificationsand variations that fall within the scope and spirit of the claimsbelow.

We claim:
 1. An isolated nucleic acid molecule, comprising a nucleotidesequence at least 90% identical to any one of SEQ ID NO: 8, SEQ ID NO:9, SEQ ID NO: 10, SEQ ID NO: 124, or SEQ ID NO:
 127. 2. The isolatednucleic acid molecule of claim 1, comprising a nucleotide sequence atleast 90% identical to SEQ ID NO:
 8. 3. The isolated nucleic acidmolecule of claim 1, comprising a nucleotide sequence at least 90%identical to SEQ ID NO:
 9. 4. The isolated nucleic acid molecule ofclaim 1, comprising a nucleotide sequence at least 90% identical to SEQID NO:
 10. 5. The isolated nucleic acid molecule of claim 1, comprisinga nucleotide sequence at least 90% identical to SEQ ID NO:
 124. 6. Theisolated nucleic acid molecule of claim 1, comprising a nucleotidesequence at least 90% identical to SEQ ID NO:
 127. 7. The isolatednucleic acid molecule of claim 1, comprising the nucleotide sequence setforth as SEQ ID NO:
 8. 8. The isolated nucleic acid molecule of claim 1,comprising the nucleotide sequence set forth as SEQ ID NO:
 9. 9. Theisolated nucleic acid molecule of claim 1, comprising the nucleotidesequence set forth as SEQ ID NO:
 10. 10. The isolated nucleic acidmolecule of claim 1, comprising the nucleotide sequence set forth as SEQID NO:
 124. 11. The isolated nucleic acid molecule of claim 1,comprising the nucleotide sequence set forth as SEQ ID NO:
 127. 12. Avector comprising the recombinant nucleic acid molecule of claim
 1. 13.The vector of claim 12, wherein the vector is a viral vector.
 14. Thevector of claim 13, wherein the viral vector is an AAV vector.
 15. Thevector of claim 12, wherein the viral vector is a gamma-retroviralvector, a lentiviral vector, or an adenoviral vector.
 16. A compositioncomprising the vector of claim 12 in a pharmaceutically acceptablecarrier.
 17. A method of inducing blood clotting in a subject in needthereof, comprising administering to the subject a therapeuticallyeffective amount of the vector of claim
 12. 18. A method of treating asubject with hemophilia B, comprising selecting a subject withhemophilia B and administering to the subject a therapeuticallyeffective amount of the vector of claim 12.